U.S. patent application number 15/443290 was filed with the patent office on 2017-08-24 for isolating cells expressing secreted proteins.
The applicant listed for this patent is Regeneron Pharmaceuticals, Inc.. Invention is credited to Thomas Aldrich, Darya Burakov, Gang Chen, Dipali Deshpande, James P. Fandl, Vishal Kamat, Neil Stahl, George D. Yancopoulos.
Application Number | 20170241887 15/443290 |
Document ID | / |
Family ID | 50233631 |
Filed Date | 2017-08-24 |
United States Patent
Application |
20170241887 |
Kind Code |
A1 |
Fandl; James P. ; et
al. |
August 24, 2017 |
Isolating Cells Expressing Secreted Proteins
Abstract
A method of detecting and isolating cells that produce a
secreted protein of interest (POI) that has an immunoglobulin CH3
domain and/or substituted CH3 domain, comprising: a) constructing a
cell line transiently or stably expressing a cell surface capture
molecule, which binds the POI, by transfecting the cell line with a
nucleic acid that encodes such cell surface capture molecule; b)
transfecting said cell simultaneously or subsequently with a second
nucleic acid that encodes a POI wherein such POI is secreted; c)
detecting the surface-displayed POI by contacting the cells with a
detection molecule, which binds the POI; and d) isolating cells
based on the detection molecule.
Inventors: |
Fandl; James P.;
(LaGrangeville, NY) ; Chen; Gang; (Yorktown
Heights, NY) ; Stahl; Neil; (Carmel, NY) ;
Yancopoulos; George D.; (Yorktown Heights, NY) ;
Deshpande; Dipali; (White Plains, NY) ; Burakov;
Darya; (Yonkers, NY) ; Aldrich; Thomas;
(Yorktown Heights, NY) ; Kamat; Vishal;
(Bergenfield, NJ) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Regeneron Pharmaceuticals, Inc. |
Tarrytown |
NY |
US |
|
|
Family ID: |
50233631 |
Appl. No.: |
15/443290 |
Filed: |
February 27, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14079699 |
Nov 14, 2013 |
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15443290 |
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13738349 |
Jan 10, 2013 |
9389236 |
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14079699 |
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12240541 |
Sep 29, 2008 |
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13738349 |
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11434403 |
May 15, 2006 |
7435553 |
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12240541 |
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11099158 |
Apr 5, 2005 |
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11434403 |
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10050279 |
Jan 16, 2002 |
6919183 |
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11099158 |
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61726040 |
Nov 14, 2012 |
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60261999 |
Jan 16, 2001 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
G01N 33/68 20130101;
G01N 2015/149 20130101; C07K 2317/52 20130101; C07K 2317/622
20130101; C07K 2317/526 20130101; C07K 16/4283 20130101; C07K
2317/31 20130101; C07K 2317/94 20130101; G01N 15/14 20130101; C07K
2317/54 20130101; C07K 2319/74 20130101; C07K 2317/92 20130101;
G01N 2015/1006 20130101; G01N 2015/0065 20130101; C07K 16/2863
20130101; C07K 2317/33 20130101; G01N 33/56966 20130101; C07K
2317/565 20130101; C07K 16/00 20130101 |
International
Class: |
G01N 15/14 20060101
G01N015/14; G01N 33/569 20060101 G01N033/569; C07K 16/00 20060101
C07K016/00; G01N 33/68 20060101 G01N033/68 |
Claims
1.-100. (canceled)
101. A method of detecting or isolating a cell that stably
expresses a protein of interest (POI) comprising the steps of: (a)
expressing in a host cell a cell surface capture protein (CSCP) and
a POI, wherein the CSCP comprises a recombinant antigen binding
protein that comprises Protein A or a functional fragment of
Protein A, (i) the CSCP binds to a first site on the POI to form a
CSCP-POI complex inside the host cell, (ii) the CSCP-POI complex is
transported through the host cell, and (iii) then displayed on the
surface of the host cell; (b) contacting the host cell with a
detection molecule, wherein the detection molecule binds to a
second site on the POI and the detection molecule comprises a heavy
chain CDR-1 (HCDR-1) having the amino acid sequence of SEQ ID
NO:32, an HCDR-2 having the amino acid sequence of SEQ ID NO:33, an
HCDR-3 having the amino acid sequence of SEQ ID NO:34, a light
chain CDR-1 (LCDR-1) having the amino acid sequence of SEQ ID
NO:35, an LCDR-2 having the amino acid sequence of SEQ ID NO:36,
and an LCDR-3 having the amino acid sequence of SEQ ID NO:37; and
(c) selecting the host cell which binds the detection molecule.
102. The method of claim 101, comprising the step of contacting the
cell with a blocking molecule prior to selecting the host cell at
step (c), wherein the blocking molecule binds to CSCP that is not
bound to the POI, but does not bind to the CSCP-POI complex.
103. The method of claim 101, wherein the selecting step (c) is
performed by fluorescence activated cell sorting.
104. The method of claim 101, wherein the POI comprises multiple
subunits and the first site on the POI resides on a first subunit,
and the second site on the POI resides on a second subunit.
105. The method of claim 104, wherein the POI protein comprises an
antibody.
106. The method of claim 104, wherein the first site on the POI
resides on a Fc domain of a heavy chain comprising a CH3 domain
that comprises (a) a histidine residue at position 95 according to
the IMGT exon numbering system, or position 435 according to the EU
numbering system and (b) a tyrosine residue at position 96
according to the IMGT exon numbering system, or position 436
according to the EU numbering system.
107. The method of claim 106, wherein the recombinant
antigen-binding protein binds a human IgG1-Fc domain, a human
IgG2-Fc domain, or a human IgG4-Fc domain.
108. The method of claim 107, wherein the recombinant
antigen-binding protein binds a polypeptide comprising the amino
acid sequence of SEQ ID NO:26.
109. The method of claim 108, wherein the recombinant
antigen-binding protein is a chimeric protein comprising the Fc
binding domain of Protein A.
110. The method of claim 109, wherein the chimeric protein
comprises the Fc binding domain of Protein A and a membrane
anchor.
111. The method of claim 110, wherein the chimeric protein
comprises the Fc binding domain of Protein A and a transmembrane
domain of an Fc receptor.
112. The method of claim 107, wherein the recombinant
antigen-binding protein binds the polypeptide with a KD of less
than about 40 nM as measured in a surface plasmon resonance
assay.
113. The method of claim 107, wherein the second site on the POI
resides on a Fc domain of a heavy chain comprising a CH3 domain
that comprises (a) an arginine residue at position 95 according to
the IMGT exon numbering system, or position 435 according to the EU
numbering system and (b) a phenylalanine residue at position 96
according to the IMGT exon numbering system, or position 436
according to the EU numbering system.
114. The method of claim 113, wherein the detection molecule binds
a human IgG1-Fc domain, a human IgG2-Fc domain, or a human IgG4-Fc
domain wherein the Fc domain comprises (a) an arginine residue at
position 95 according to the IMGT exon numbering system, or
position 435 according to the EU numbering system and (b) a
phenylalanine residue at position 96 according to the IMGT exon
numbering system, or position 436 according to the EU numbering
system.
115. The method of claim 114, wherein the detection molecule
comprises a labeled anti-human IgG F(ab')2.
116. The method of claim 114, wherein the detection molecule binds
a polypeptide comprising an amino acid sequence of SEQ ID
NO:42.
117. The method of claim 114, wherein detection molecule binds the
polypeptide with a KD of less than about 60 nM as measured in a
surface plasmon resonance assay.
118. The method of claim 114, wherein the detection molecule
comprises an HCVR having an amino acid sequence that is at least
95% identical to SEQ ID NO:38 and an LCVR having an amino acid
sequence that is at least 95% identical to SEQ ID NO:39.
119. The method of claim 114, wherein the detection molecule
comprises an HCVR having the amino acid sequence of SEQ ID NO:38
and an LCVR having the amino acid sequence of SEQ ID NO:39.
120. The method of claim 114, wherein the detection molecule
comprises an antibody comprising a heavy chain comprising an amino
acid sequence that is at least 95% identical to SEQ ID NO:40 and a
light chain comprising an amino acid sequence that is at least 95%
identical to SEQ ID NO:41.
121. The method of claim 114, wherein the antibody comprises a
heavy chain that has an amino acid sequence identical to SEQ ID
NO:40 and a light chain that has an amino acid sequence identical
to SEQ ID NO:41.
122. The method of claim 114, wherein the detection molecule
comprises an ScFv fusion protein comprising (a) a heavy chain
variable domain comprising an amino acid sequence that is at least
95% identical to SEQ ID NO:38, (b) a light chain variable domain
comprising an amino acid sequence that is at least 95% identical to
SEQ ID NO:39, and (c) a membrane anchor domain.
123. The method of claim 114, wherein the detection molecule
comprises an ScFv fusion protein comprising a heavy chain variable
domain that has an amino acid sequence identical to SEQ ID NO:38
and a light chain variable domain that has an amino acid sequence
identical to SEQ ID NO:39.
124. The method of claim 114, wherein the detection molecule
comprises an ScFv fusion protein comprising the amino acid sequence
of SEQ ID NO:43.
125. The method of claim 102, wherein the blocking molecule is a
non-human IgG.
126. The method of claim 102, wherein the blocking molecule is an
human Fc molecule.
127. A method of producing a bispecific antibody comprising: (a)
expressing in a host cell (i) a cell surface capture protein
("CSCP"), wherein the CSCP comprises a first recombinant antigen
binding protein that comprises Protein A or a functional fragment
of Protein A (ii) an antibody light chain, (iii) a first antibody
heavy chain comprising a CH3 domain comprising a histidine at IMGT
position 95 and a tyrosine at IMGT position 96, or position 435
according to the EU numbering system, and (iv) a second antibody
heavy chain comprising a CH3 domain comprising an arginine at IMGT
position 95 and a phenylalanine at IMGT position 96, or position
436 according to the EU numbering system, wherein inside the host
cell (1) the CSCP binds to the first antibody heavy chain but does
not bind to the second antibody heavy chain, (2) the second
antibody heavy chain binds to the first antibody heavy chain, and
(3) one antibody light chain binds to the first antibody heavy
chain and another antibody light chain binds to the second antibody
heavy chain, to form a ternary complex, then (4) the ternary
complex is presented on the host cell surface; (b) contacting the
cell with a blocking molecule, which binds to a CSCP that is not
bound to a first antibody heavy chain; (c) contacting the cell with
a detection molecule ("DM"), which binds to the second antibody
heavy chain; (d) selecting and pooling the host cells that bind the
DM.
128. The method of claim 127, wherein the selected and pooled host
cells of step (d) are (e) cultured and expanded; and then (f)
subjected to steps (a)-(d) again to obtain an enriched pool of host
cells that produce a bispecific antibody.
129. The method of claim 128, wherein steps (e) and (f) are
performed one or more times.
130. A system comprising a host cell, wherein the cell comprises:
(a) a CSCP polynucleotide encoding an cell surface capture protein
(CSCP) that specifically binds a human IgG1-Fc domain, a human
IgG2-Fc domain, or a human IgG4-Fc domain; wherein (i) the CSCP
comprises a membrane anchor, (ii) the CSCP is positioned at the
plasma membrane of the cell, and (iii) the CSCP binds to an IgG
molecule such that the IgG molecule is exposed to the outside of
the cell; and (b) an IgG polynucleotide encoding the IgG
molecule.
131. The system of claim 130, wherein the CSCP binds to a domain
comprising (a) a histidine residue at position 95 according to the
IMGT exon numbering system, or position 435 according to the EU
numbering system and (b) a tyrosine residue at position 96
according to the IMGT exon numbering system, or position 436
according to the EU numbering system.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of, and claims priority
under 35 U.S.C. .sctn.120, to U.S. patent application Ser. No.
14/079,699 filed Nov. 14, 2013, which is a continuation-in-part of
U.S. patent application Ser. No. 13/738,349, filed Jan. 10, 2013,
now U.S. Pat. No. 9,389,236, which is a continuation of U.S. patent
application Ser. No. 12/240,541, filed Sep. 29, 2008, now
abandoned, which is a continuation-in-part of U.S. patent
application Ser. No. 11/434,403 filed May 15, 2006, now U.S. Pat.
No. 7,435,553, which is a continuation of U.S. patent application
Ser. No. 11/099,158 filed Apr. 5, 2005, now abandoned, which is a
divisional of U.S. patent application Ser. No. 10/050,279 filed
Jan. 16, 2002, now U.S. Pat. No. 6,919,183. This application also
claims priority under 35 U.S.C. .sctn.119(e) to U.S. Provisional
Patent Application No. 61/726,040 filed Nov. 14, 2012 and to U.S.
Provisional Patent Application No. 60/261,999 filed Jan. 16, 2001.
The entire contents of the aforementioned applications are
incorporated herein by reference.
BACKGROUND
Sequence Listing
[0002] This application incorporates by reference the Sequence
Listing submitted in Computer Readable Form as file 790F_ST25.txt
created on Oct. 23, 2013 (86,532 bytes).
FIELD OF THE INVENTION
[0003] The field of this invention is a method for identifying and
isolating cells that produce secreted proteins. More specifically,
the method allows rapid isolation of high expression recombinant
antibody-producing cell lines, including rapid isolation of
specific hybridomas. The methods also allow for the rapid and
efficient isolation of cells secreting heterodimeric proteins, e.g.
bispecific antibodies, thereby enriching the heterodimeric species
(bispecific molecule) and preferentially isolating the
heterodimeric from the homodimeric species.
[0004] Prior art methods for expressing a gene of interest (GOI) in
a host cell are known. Briefly, an expression vector carrying the
GOI is introduced into the cell. Following stable integration,
standard methods for isolating high expression cells involve
collection of cell pools, hand-picking colonies from plates,
isolation of single cells by limited dilution, or other methods
known in the art. Pools or individual clones are then expanded and
screened for production of the protein of interest (POI) by direct
measurement of POI activity, by immunological detection of POI, or
by other suitable techniques. These procedures are laborious,
inefficient, expensive, and the number of clones that can be
analyzed is usually limited to a few hundred.
[0005] The large degree of heterogeneity in protein expression by
cells following stable integration requires that many individual
clones be screened in an effort to identify the rare integration
event that results in a stable, high expression production cell
line. This requirement calls for methods that enable rapid
identification and isolation of cells expressing the highest level
of protein production. Moreover, the collection of clone pools or
hand-picked colonies risks losing high expression cells, which
often grow more slowly, to faster growing low expression cells.
Therefore, a need exists for methods that allow rapid screening and
isolation of individual cells capable of high level expression of a
secreted POI. Where the POI contains more than one subunit, it is
necessary to select preferentially for a desired heterodimeric
species versus a homodimeric species.
[0006] Incorporation of flow cytometry into methods used for the
isolation of stable expression cell lines has improved the
capability of screening large numbers of individual clones,
however, currently available methods remain inadequate for diverse
reasons. Diffusion of the POI between cells of different
characteristics was also a problem.
BRIEF SUMMARY
[0007] The present invention describes a high-throughput screening
method for the rapid isolation of those cells that secrete protein
by directly screening for the protein of interest (POI). This
invention also allows for the convenient monitoring of POI
expression on a single-cell basis during the manufacturing process.
Furthermore, this technology can be directly applied to screening
of antibody-producing cells, such as bispecific antibody-producing
cells, or any cell producing a heterodimeric protein. The
technology can also be directly applied to screening of cells
producing modified T cell receptors, such as, for example, cells
that produce soluble forms of T cell receptors.
[0008] In one aspect, the invention provides a method of detecting
and isolating cells that produce a secreted protein of interest
(POI), comprising: a) constructing a nucleic acid molecule that
encodes a cell surface capture molecule capable of binding a POI;
b) transfecting a cell expressing the POI with the nucleic acid
molecule of step a); c) detecting the surface-displayed POI by
contacting the cells with a detection molecule, where in the
detection molecule binds the POI; and d) isolating cells based on
the detection molecule.
[0009] In various embodiments, the protein of interest includes a
ligand, a soluble receptor protein, a growth factor, a fusion
protein, an antibody, a bispecific antibody, an Fab, a single chain
antibody (ScFv), or a fragment thereof. When the protein of
interest is an antibody, the antibody is selected from the group
consisting of IgM, IgG, IgA, IgD or IgE, as well as various
subtypes or variants of these. In a specific embodiment, the
antibody is an anti-DII4 antibody, an anti-ErbB3 antibody, an
anti-EGFR antibody, a dual-specific anti-ErbB3/EGFR bispecific
antibody, or an anti-IL-6 receptor antibody.
[0010] In more specific embodiments, the protein of interest is a
growth factor selected from the group consisting of Interleukin
(IL)-1, IL-2, IL-4, IL-5, IL-6, IL-7, IL-9, IL-10, IL-13, IL-15,
IL-16, IL-17, IL-18, IL-21, Ciliary Neurotrophic Factor (CNTF),
erythropoietin, Vascular Endothelial Growth Factor (VEGF),
angiopoietin 1 (Ang-1), angiopoietin 2 (Ang-2), TNF,
Interferon-gamma, GM-CSF, TGF.beta., and TNF Receptor.
[0011] In various embodiments, the protein of interest comprises a
variable domain of a T cell receptor. In specific embodiments, the
protein of interest is a soluble T cell receptor (sTCR), or a
protein comprising a T cell receptor extracellular domain fused to
an Fc (TCR-Fc), In a specific embodiment, the Fc is a human Fc. In
various embodiments, the protein comprises a variable domain of a T
cell receptor extracellular domain. In various embodiments, the
protein comprises a variable domain and a constant region of a T
cell receptor extracellular domain.
[0012] The nucleic acid that encodes the protein of interest may be
from any source, naturally occurring or constructed through
recombinant technology, and may be selected from a DNA library.
[0013] In various embodiments, the cell surface capture molecule is
a ligand-specific receptor, a receptor-specific ligand, an
antibody-binding protein, an antibody or antibody fragment, such as
an ScFv, or a peptide. When the capture molecule is a peptide, the
peptide may be isolated from a phage display library. In more
specific embodiments, the capture molecule may be Ang1, Ang2, VEGF,
Tie1, Tie2, VEGFRI (Flt1), VEGFRII (Flk1 or KDR), CNTF,
CNTFR-.alpha., cytokine receptor components, fusions of two or more
cytokine receptor components, or a fragment thereof. When the
capture molecule is an antibody-binding protein, the
antibody-binding protein may be an Fc receptor, an
anti-immunoglobulin antibody, an anti-immunoglobulin (anti-Ig)
ScFv, an anti-Fc antibody, anti-Fc* antibody, Protein A, Protein L,
Protein G, Protein H or functional fragments thereof. As such, in
some embodiments, the capture molecule is a fusion protein
comprising an antigen, Protein A, or anti-Ig ScFv fused to a
transmembrane domain or a GPI linker.
[0014] In some embodiments where the protein of interest is a
heterodimeric protein, such as a heterodimeric protein having a
first subunit and a second subunit, the cell surface capture
molecule comprises an antigen, Protein A, or ScFv capable of
binding the first subunit and not the second subunit, or such cell
surface capture molecule binds the second subunit and not the first
subunit.
[0015] In various embodiments where the protein of interest
comprises a T cell receptor variable domain, the cell surface
capture molecule comprises an Fc receptor or a membrane-associated
antigen capable of being recognized by the variable domain of the T
cell receptor.
[0016] In various embodiments where the protein of interest is an
IgG1, IgG2, IgG4, or a bispecific antibody having one CH3 domain
comprising a mutation the abrogates binding to protein A and the
other CH3 domain capable of binding to protein A; or a fusion
protein comprising an Fc region from IgG1, IgG2, IgG4, or an Fc
region having one CH3 domain comprising a mutation that abrogates
binding to protein A and the other CH3 domain capable of binding to
protein A, the cell surface capture molecule comprises an
anti-immunoglobulin ScFv, such as an anti-Fc or anti-Fc* ScFv.
[0017] In several embodiments, the methods of the invention further
comprise a membrane anchor that serves to anchor the POI to the
cell membrane, exposed to the outside of the cell, and thus
functions as a cell surface capture molecule. In specific
embodiments, the membrane anchor is a transmembrane anchor or a GPI
link. Examples of specific transmembrane anchors include the
transmembrane domain of an Fc receptor, such as the transmembrane
domain of human Fc.gamma.RI, an example of which is cited in SEQ ID
NO:17. The membrane anchor may be native to the cell, recombinant,
or synthetic.
[0018] In various embodiments, the protein of interest comprises a
T cell receptor variable region, and the cell surface capture
molecule comprises a membrane-associated antigen. In a specific
embodiment, the membrane-associated antigen is a recombinant fusion
protein comprising an antigen capable of being recognized by the T
cell receptor variable region fused to a membrane anchor wherein
the antigen is associated with the cell surface. In a specific
embodiment, the recombinant fusion protein comprises an antigen
fused to a transmembrane anchor or a GPI link. In another specific
embodiment, the cell surface capture molecule comprises a
recombinant fusion protein comprising an membrane anchor and an
antigen that is capable of binding to a major histocompatibility
(MHC) molecule, including but not limited to, for example, tumor
antigens and self proteins of transformed phenotype.
[0019] In further embodiments, a signal sequence is added to the
amino terminus of a POI, such that the protein is transported to
the cell surface, and functions as a cell surface capture molecule.
The signal sequence may be native to the cell, recombinant, or
synthetic.
[0020] In various embodiments, a blocking molecule which binds the
cell surface capture molecule is added to reduce the diffusion of
the POI from the expressing cell to a neighboring cell. In another
embodiment, the diffusion of the POI from the expressing cell to a
neighboring cell and its adherence to that cell is reduced by
increasing the viscosity of the media.
[0021] The cell isolated by the methods of the invention may be an
antibody-producing cell fused to an immortalized cell. In more
specific embodiments, the antibody-producing cell is a B-cell or
derivative thereof. A B-cell derivative may be a plasma cell, a
hybridoma, a myeloma, or a recombinant cell.
[0022] In addition, the methods of the invention are useful for
identification of B-cells and derivatives thereof, or hybridomas
that express secreted antibodies of a desired specificity, affinity
or isotype. The invention can also be used for isolation of cells
that express desired levels of an antibody or antibody
fragments.
[0023] Detection of the cells with the displayed POI may be
accomplished through the use of any molecule capable of directly or
indirectly binding the displayed POI. Such detection molecules may
facilitate the detection and/or isolation of the cells displaying
the POI. In one embodiment, two molecules that bind each other and
are deferentially labeled are utilized. The detection and/or
isolation may be accomplished through standard techniques known in
the art.
[0024] In another aspect, the invention features a method of
detecting and isolating cells that produce a secreted protein of
interest (POI), comprising: a) transfecting a cell with a nucleic
acid that encodes a cell surface capture molecule, wherein the cell
surface capture molecule is capable of binding the POI; b)
transfecting the cell of a) simultaneously or subsequently with a
second nucleic acid that encodes a POI wherein the POI is expressed
and secreted; c) detecting the surface-displayed POI by contacting
the cell with a detection molecule, which binds the POI; and d)
isolating cells based on the detection molecule.
[0025] In another aspect, the invention features a method of
detecting and isolating cells that produce a POI, comprising: a)
detecting a cell that expresses a cell surface capture molecule in
high yield; b) isolating and culturing the cell detected in (a); c)
transfecting the cell in (b) with a nucleic acid that encodes a POI
wherein such POI is secreted; d) detecting the surface-displayed
POI by contacting the cells with a detection molecule which binds
the POI; and e) isolating cells based on the detection
molecule.
[0026] In another aspect, the invention provides a method of
detecting and isolating cells that produce high levels of protein
of interest (POI), comprising: a) transfecting cells with a nucleic
acid that encodes such cell surface capture molecule capable of
binding the POI, wherein the cell expresses the POI; b) detecting a
cell from (a) that expresses said cell surface capture molecule in
high yield; c) isolating and culturing a high yield cell; d)
detecting the surface-displayed POI by contacting the cell with a
detection molecule binds the POI; and e) isolating the detected
cell.
[0027] In another aspect, the invention provides a method of
detecting and isolating cells that produce high levels of a
heterodimeric protein, comprising: (a) transfecting cells with a
nucleic acid that encodes a cell surface capture molecule, which is
a fusion protein comprising a membrane anchor domain and is capable
of binding a first subunit of the heterodimeric protein, wherein
the cell expresses the heterodimeric protein; (b) detecting a cell
of (a) that expresses the surface capture molecule in high yield;
(c) isolating and culturing the cell that expresses the surface
capture molecule in high yield; (d) detecting the heterodimeric
protein on the surface of the isolated and cultured cell of step
(c) with a detection molecule that binds a second subunit of the
heterodimeric protein; and (e) isolating the cell detected in step
(d) that bears the detected heterodimeric protein on its
surface.
[0028] In another aspect, the invention provides a method of
detecting and isolating cells that produce high levels of an
immunoglobulin, comprising: (a) transfecting cells with a nucleic
acid that encodes a cell surface capture molecule capable of
binding the immunoglobulin, wherein the cell expresses the
immunoglobulin; (b) detecting a cell of (a) that expresses the
surface capture molecule in high yield; (c) isolating and culturing
the cell that expresses the surface capture molecule in high yield;
(d) detecting the immunoglobulin on the surface of the isolated and
cultured cell of step (c) with a detection molecule that binds the
immunoglobulin; and (e) isolating the cell detected in step (d)
that bears the detected immunoglobulin on its surface.
[0029] In some of these methods the heterodimeric protein or
immunoglobulin is an antibody, and the first subunit of the
heterodimeric proteinor immunoglobulin comprises a heavy chain
domain comprising a wild type CH3 domain. In certain embodiments,
the CH3 domain comprises a histidine residue at position 95
according to the IMGT exon numbering system and a tyrosine residue
at position 96 according to the IMGT exon numbering system.
[0030] In another aspect, the invention provides a method of
detecting and isolating cells that produce high levels of a
bispecific antibody, comprising: (a) transfecting cells with a
nucleic acid that encodes a cell surface capture molecule, which is
a fusion protein comprising a membrane anchor domain, such as an
ScFv fusion protein, and is capable of binding the bispecific
antibody, wherein the cell expresses the bispecific antibody; (b)
detecting a cell of (a) that expresses the surface capture molecule
in high yield; (c) isolating and culturing the cell that expresses
the surface capture molecule in high yield; (d) detecting the
bispecific antibody on the surface of the isolated and cultured
cell of step (c) with a detection molecule that binds the
bispecific antibody; and (e) isolating the cell detected in step
(d) that bears the detected bispecific antibody on its surface.
[0031] In another aspect, a method for detecting cells that produce
a desired level of an affinity agent that comprises a T-cell
receptor (TCR) variable region is provided.
[0032] In another aspect, a method for detecting cells that produce
a desired level of a TCR-Fc is provided, comprising: (a)
transfecting cells with a nucleic acid that encodes an Fc receptor
capable of binding a TCR-Fc, wherein the cell expresses an antigen
recognized by the TCR-Fc; (b) detecting a cell of (a) that
expresses the TCR-Fc in high yield; (c) isolating and culturing the
cell that expresses the TCR-Fc in high yield; (d) detecting the
antigen on the surface of the isolated and cultured cell of step
(c) with a detection molecule; and (e) isolating the cell detected
in step (d) that bears the detected antigen on its surface.
[0033] In various embodiments, the TCR is selected from a human TCR
and a rodent TCR such as a rat, mouse, or hamster TCR. In a
specific embodiment the Fc is a human Fc. In another specific
embodiment, the Fc is a human Fc and the Fc receptor is a high
affinity human Fc receptor. In a specific embodiment, the high
affinity human Fc receptor is a human Fc.gamma.RI.
[0034] In various embodiments, the cell surface capture protein is
surface-bound antigen. In a specific embodiment, the antigen is
bound to the surface by fusion to a transmembrane domain or a GPI
linker.
[0035] In some aspects of the method for selecting enhanced cells
that produce a protein of interest, recombinant antigen-binding
proteins can be used as cell surface capture proteins (CSCP),
detection molecules (DM), and/or blocking molecules. Therefore, the
invention provides recombinant antigen-binding proteins.
[0036] In one aspect, the invention provides a recombinant
antigen-binding protein that binds a human IgG1-Fc domain, a human
IgG2-Fc domain, or a human IgG4-Fc domain, or any protein that
comprises for example an amino acid sequence of SEQ ID NO:26, which
encodes a human Fc. In some embodiments, the recombinant
antigen-binding protein binds the polypeptide with a K.sub.D of
less than about 40 nM as measured in a surface plasmon resonance
assay.
[0037] In some embodiments, the recombinant antigen-binding protein
comprises one or more complementarity determining regions (CDRs) of
a heavy chain variable region (HCVR) having an amino acid sequence
that is at least 95% identical to SEQ ID NO:15, or of a light chain
variable region (LCVR) having an amino acid sequence that is at
least 95% identical to SEQ ID NO:16. In one case, the protein
comprises a heavy chain CDR-1 (HCDR-1) having the amino acid
sequence of SEQ ID NO:27, an HCDR-2 having the amino acid sequence
of SEQ ID NO:28, an HCDR-3 having the amino acid sequence of SEQ ID
NO:29, a light chain CDR-1 (LCDR-1) having the amino acid sequence
of SEQ ID NO:30, and an LCDR-2 having the amino acid sequence of
SEQ ID NO:31. In some cases, the protein comprises an HCVR having
an amino acid sequence that is at least 95% identical to SEQ ID
NO:15 (some of which are identical to SEQ ID NO:15) and an LCVR
having an amino acid sequence that is at least 95% identical to SEQ
ID NO:16 (some of which are identical to SEQ ID NO:16).
[0038] Recombinant antigen-binding proteins, which are antibodies,
are useful as detection molecules (DMs).
[0039] In some embodiments, the recombinant antigen-binding protein
is an ScFv fusion protein, which in some cases comprises a heavy
chain variable domain with an amino acid sequence that is at least
95% identical to (or identical to) SEQ ID NO:15, a light chain
variable domain with an amino acid sequence that is at least 95%
identical to (or identical to) SEQ ID NO:16, and a membrane anchor
domain. In one embodiment, the membrane anchor domain is derived
from an Fc receptor, such as the transmembrane domain of the human
Fc.gamma.R1 protein, as represented by SEQ ID NO:17, or SEQ ID
NO:21, which contains not only the transmembrane domain, but also
the C-terminal cytoplasmic domain (SEQ ID NO:18). In one specific
embodiment, the ScFv fusion protein has the amino acid sequence of
SEQ ID NO:19. Recombinant antigen-binding proteins, which are ScFv
fusion proteins, are useful as CSCPs and as DMs.
[0040] In another aspect, the invention provides a polynucleotide
that encodes the antigen-binding protein of the preceding aspect.
In one embodiment, such as in the case where the antigen-binding
protein is an antibody, the polynucleotide encodes the light chain.
Likewise, the polynucleotide may encode the heavy chain. In the
case in which the antigen-binding protein is an ScFv fusion
protein, the polynucleotide may encode the ScFv-Fc.gamma.RTM-cyto
fusion protein of SEQ ID NO:19. For example, the polynucleotide of
SEQ ID NO: 20 encodes SEQ ID NO:19.
[0041] In another aspect, the invention provides a nucleic acid
vector that encompasses the polynucleotide of the preceding aspect.
In one embodiment, the vector comprises the polynucleotide, which
encodes the antigen-binding protein, operably linked to an upstream
promoter, and followed by a downstream polyadenylation sequence.
The promoter can be any promoter, such as for example a CMV
promoter. Thus in one case, the vector may contain the sequence of
SEQ ID NO:25. In one embodiment, the vector may contain a nucleic
acid sequence that encodes a selectable marker, such as for example
neomycin resistance. In one embodiment, the vector may contain a
nucleic acid sequence that encodes an energy transfer protein, such
as green fluorescence protein (GFP), or a derivative thereof, such
as yellow fluorescence protein (YFP). Thus in one case, the vector
may contain the sequence of SEQ ID NO:24.
[0042] The vector may be circular or linear, episomal to a host
cell's genome or integrated into the host cell's genome. In some
embodiments, the vector is a circular plasmid, which in one
specific embodiment has the nucleic acid sequence of SEQ ID NO:23
for the ScFv-Fc.gamma.R-TM-cyto-encoding polynucleotide, in another
specific embodiment comprises the nucleic acid sequence of the
antibody heavy chain-encoding polynucleotide, and yet another
specific embodiment comprises the nucleic acid sequence of the
antibody light chain-encoding polynucleotide. In some embodiments,
the vector is a linear construct, which may be integrated into a
host cell chromosome. In one specific embodiment, the linear
construct has the nucleic acid sequence of SEQ ID NO:22 for the
ScFv-Fc.gamma.R-TM-cyto-encoding polynucleotide. In another
specific embodiment, the linear construct comprises the nucleic
acid sequence of the antibody heavy chain-encoding polynucleotide.
In yet another specific embodiment, the linear construct comprises
the nucleic acid sequence of the antibody light chain-encoding
polynucleotide.
[0043] The host cell may be any cell, prokaryotic or eukaryotic.
However, in one specific embodiment, the host cell is a CHO cell,
such as a CHO-K1 cell.
[0044] In another aspect, the invention provides a host cell that
expresses the antigen-binding protein of the preceding aspect,
and/or contains the polynucleotide or nucleic acid vector of the
preceding aspects. In some embodiments, the host cell is a CHO
cell. In a specific embodiment, the host cell is a CHO-K1 cell. In
one embodiment, host cell is used in the production of a protein of
interest, and the antigen-binding protein is used as a cell surface
capture protein according to the methods disclosed in this
application.
[0045] In one aspect, the invention provides a host cell useful in
the production of a protein of interest. The host cell harbors a
polynucleotide or nucleic acid vector of a preceding aspect, and
produces an antigen-binding protein of a preceding aspect, which
serves as a cell surface capture protein. The cell surface capture
protein binds to the protein of interest inside the host cell, and
is transported through the secretory apparatus of the cell, and is
expressed on the surface of the host cell. Thus, in one embodiment,
the host cell comprises a cell surface capture protein positioned
in the host cell plasma membrane, with the capturing moiety facing
outside of the cell. In one embodiment, the cell surface capture
molecule is bound to a protein of interest, which is positioned at
the plasma membrane and oriented outside of the cell.
[0046] In one embodiment, the host cell produces or is capable of
producing an ScFv fusion protein that binds to a protein of
interest that contains an Fc domain, which contains a histidine at
IMGT position 95 and a tyrosine at IMGT position 96. Examples
include IgG1, IgG2, and IgG4 proteins. In one embodiment, the ScFv
fusion protein contains amino acid sequences set forth in SEQ ID
NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, and SEQ ID NO:31.
In one specific embodiment, the ScFv fusion protein comprises the
amino acid sequence of SEQ ID NO:19. In a specific embodiment, the
host cell comprises a cell surface capture protein positioned at
the plasma membrane and bound to an IgG1, IgG2 or IgG4, or a
bispecific antibody containing at least one heavy chain of an IgG1,
lgG2 or IgG4, and which may have a second heavy chain that is of
another type or contains one of more amino acid substitutions.
[0047] In one aspect, the invention provides a recombinant
antigen-binding protein that binds a substituted CH3 polypeptide
comprising one or more amino acid substitutions selected from the
group consisting of (a) 95R, and (b) 95R and 96F according to the
IMGT exon numbering system, or (a') 435R, and (b') 435R and 436F
according to the EU numbering system, or any protein that comprises
for example an amino acid sequence of SEQ ID NO:42, which encodes a
substituted human Fc (also known as Fc*). In some embodiments, the
recombinant antigen-binding protein binds the polypeptide with a
K.sub.D of less than about 60 nM as measured in a surface plasmon
resonance assay.
[0048] In some embodiments, the recombinant antigen-binding protein
comprises one or more complementarity determining regions (CDRs) of
a heavy chain variable region (HCVR) having an amino acid sequence
that is at least 95% identical to SEQ ID NO:38, or of a light chain
variable region (LCVR) having an amino acid sequence that is at
least 95% identical to SEQ ID NO:39. In one case, the protein
comprises a heavy chain CDR-1 (HCDR1) having the amino acid
sequence of SEQ ID NO:32, an HCDR-2 having the amino acid sequence
of SEQ ID NO:33, an HCDR-3 having the amino acid sequence of SEQ ID
NO:34, a light chain CDR-1 (LCDR-1) having the amino acid sequence
of SEQ ID NO:35, and an LCDR-2 having the amino acid sequence of
SEQ ID NO:36. In some cases, the protein comprises an HCVR having
an amino acid sequence that is at least 95% identical to SEQ ID
NO:38 (some of which are identical to SEQ ID NO:38) and an LCVR
having an amino acid sequence that is at least 95% identical to SEQ
ID NO:39 (some of which are identical to SEQ ID NO:39).
[0049] In some embodiments, the recombinant antigen-binding protein
is an antibody, which comprises a heavy chain and a light chain.
The heavy chain may comprise an amino acid sequence that is at
least 95% identical to (or 100% identical to) SEQ ID NO:40. The
light chain may comprise an amino acid sequence that is at least
95% identical to (or 100% identical to) SEQ ID NO:41. Recombinant
antigen-binding proteins, which are antibodies, are useful as
detection molecules (DMs).
[0050] In some embodiments, the recombinant antigen-binding protein
is an ScFv fusion protein, which in some cases comprises a heavy
chain variable domain with an amino acid sequence that is at least
95% identical to (or identical to) SEQ ID NO:38, a light chain
variable domain with an amino acid sequence that is at least 95%
identical to (or identical to) SEQ ID NO:39, and a membrane anchor
domain. In one embodiment, the membrane anchor domain is derived
from an Fc receptor, such as the transmembrane domain of the human
Fc.gamma.R1 protein, as represented by SEQ ID NO:17, or SEQ ID
NO:21, which contains not only the transmembrane domain, but also
the C-terminal cytoplasmic domain of SEQ ID NO:19. In one specific
embodiment, the ScFv fusion protein has the amino acid sequence of
SEQ ID NO:43. Recombinant antigen-binding proteins, which are ScFv
fusion proteins, are useful as CSCPs and as DMs.
[0051] In another aspect, the invention provides a polynucleotide
that encodes the antigen-binding protein of the preceding aspect.
In one embodiment, such as in the case where the antigen-binding
protein is an antibody, the polynucleotide encodes the light chain,
such as for example the light chain of SEQ ID NO:41. Likewise, the
polynucleotide may encode the heavy chain, such as for example, the
heavy chain of SEQ ID NO:40. In the case in which the
antigen-binding protein is an ScFv fusion protein, the
polynucleotide may encode the ScFv-Fc.gamma.R-TM-cyto fusion
protein of SEQ ID NO:43. Representative exemplar polynucleotides
include those polynucleotides of SEQ ID NO:49, 50 and 51,
respectively.
[0052] In another aspect, the invention provides a nucleic acid
vector that encompasses the polynucleotide of the preceding aspect.
In one embodiment, the vector comprises the polynucleotide, which
encodes the antigen-binding protein, operably linked to an upstream
promoter, and followed by a downstream polyadenylation sequence.
The promoter can be any promoter, such as for example a CMV
promoter. Thus in one case, the vector may contain the sequence of
SEQ ID NO:47. In one embodiment, the vector may contain a nucleic
acid sequence that encodes a selectable marker, such as for example
neomycin resistance. In one embodiment, the vector may contain a
nucleic acid sequence that encodes an energy transfer protein, such
as green fluorescence protein (GFP), or a derivative thereof, such
as yellow fluorescence protein (YFP). Thus in one case, the vector
may contain the sequence of SEQ ID NO:46.
[0053] The vector may be circular or linear, episomal to a host
cell's genome or integrated into the host cell's genome. In some
embodiments, the vector is a circular plasmid, which in one
specific embodiment has the nucleic acid sequence of SEQ ID NO:44
for the ScFv-Fc.gamma.R-TM-cyto-encoding polynucleotide, in another
specific embodiment has the nucleic acid sequence of the antibody
heavy chain-encoding polynucleotide, and yet another specific
embodiment has the nucleic acid sequence of the antibody light
chain-encoding polynucleotide. In some embodiments, the vector is a
linear construct, which may be integrated into a host cell
chromosome. In one specific embodiment, the linear construct
comprises the nucleic acid sequence of SEQ ID NO:51 for the
ScFv-Fc.gamma.R-TM-cyto-encoding polynucleotide. In another
specific embodiment, the linear construct comprises the nucleic
acid sequence of SEQ ID NO:50 for the antibody heavy chain-encoding
polynucleotide. In yet another specific embodiment, the linear
construct comprises the nucleic acid sequence of SEQ ID NO:49 for
the antibody light chain-encoding polynucleotide.
[0054] The host cell may be any cell, prokaryotic or eukaryotic.
However, in one specific embodiment, the host cell is a CHO cell,
such as a CHO-K1 cell.
[0055] In another aspect, the invention provides a host cell that
expresses the antigen-binding protein of the preceding aspect,
and/or contains the polynucleotide or nucleic acid vector of the
preceding aspects. In some embodiments, the host cell is a CHO
cell. In a specific embodiment, the host cell is a CHO-K1 cell. In
one embodiment, host cell is used in the production of a protein of
interest, and the antigen-binding protein is used as a cell surface
capture protein according to the methods disclosed in this
application.
[0056] In one aspect, the invention provides a host cell useful in
the production of a protein of interest. The host cell harbors a
polynucleotide or nucleic acid vector of a preceding aspect, and
produces an antigen-binding protein of a preceding aspect, which
serves as a cell surface capture protein. The cell surface capture
protein binds to the protein of interest inside the host cell, and
is transported through the secretory apparatus of the cell, and is
expressed on the surface of the host cell. Thus, in one embodiment,
the host cell comprises a cell surface capture protein positioned
in the host cell plasma membrane, with the capturing moiety facing
outside of the cell. In one embodiment, the cell surface capture
molecule is bound to a protein of interest, which is positioned at
the plasma membrane and oriented outside of the cell.
[0057] In one embodiment, the host cell produces or is capable of
producing an ScFv fusion protein that binds to a protein of
interest that contains an Fc domain, which contains an arginine at
IMGT position 95 and a phenylalanine at IMGT position 96 (Fc*).
Examples include IgG3 and substituted CH3 regions of IgG1, IgG2,
and IgG4 proteins. In one embodiment, the ScFv fusion protein
contains amino acid sequences set forth in SEQ ID NO:32, SEQ ID
NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36 and SEQ ID NO:37.
In one specific embodiment, the ScFv fusion protein comprises the
amino acid sequence of SEQ ID NO:43. In a specific embodiment, the
host cell comprises a cell surface capture protein positioned at
the plasma membrane and bound to an IgG3 or a substituted IgG1,
IgG2 or IgG4, which contain the arginine at IMGT position 95 and
phenylalanine at IMGT position 96 ("Fc*"), or a bispecific antibody
containing at least one heavy chain of a the Fc* type and the other
heavy chain of the IgG1, IgG2 or IgG4 wildtype.
[0058] In another aspect, the invention provides a method of
detecting, isolating, or enriching for a cell that stably expresses
a protein of interest (POI). The method includes the step of
expressing in the host cell a cell surface capture protein (CSCP)
and a POI. According to this method, the CSCP binds to a "first
site" on the POI to form a CSCP-POI complex inside the host cell.
This CSCP-POI complex is then transported through the secretory
system of the host cell, and is secreted from the cell. Since the
CSCP contains a membrane binding domain (e.g., SEQ ID NO:17), the
CSCP-POI complex is displayed on the surface of the host cell, with
the POI exposed outside of the cell. According to the method, the
host cell is then contacted with a detection molecule (DM), which
binds to a "second site" on the POI. Those cells that bind the DM
are selected for identification, isolation, pooling, and/or
enrichment. In one embodiment, the DM-bound host cell is selected
by fluorescence activated cell sorting.
[0059] In one embodiment, the method also includes the step of
contacting the cell with a blocking molecule prior to selecting the
host cell. The blocking molecule binds to any CSCP that is not
bound to the POI. The blocking molecule does not bind to the
CSCP-POI complex.
[0060] In some embodiments, the POI contains multiple subunits,
such as an antibody that comprises two heavy chains and two light
chains. In that case, the first site on the POI may reside on a
first subunit, and the second site on the POI may reside on a
second subunit. In some embodiments, the POI contains multiple
subunits, such as a heterodimeric protein. In the case of a
heterodimeric protein, the first site on the POI may reside on a
first subunit, such as a first receptor, and the second site on the
POI may reside on a second subunit, such as a second receptor or
coreceptor. In some embodiments, the heterodimeric proteins are
different receptors that interact to form the heterodimer. Where
the POI is an antibody, the first site on the POI may reside on a
first heavy chain, and the second site on the POI may reside on a
second heavy chain. In some embodiments, the antibody contains
subunits that differ by at least one amino acid, such as an
antibody having at least one heavy chain with a wild type CH3
domain and the other heavy chain having at least one amino acid
substitution in the CH3 domain. In this case, the CSCP may be an
antigen-binding protein as described herein, such as an antigen or
anti-Ig ScFv fusion protein. Here, the detection molecule (DM) may
comprise a labeled recombinant antigen-binding protein as described
herein, such as a labeled antigen or anti-Ig antibody or ScFv
molecule.
[0061] In some cases, for example where the POI is a bispecific
antibody, the first site may reside on a heavy chain that has a CH3
domain containing a histidine residue at position 95 according to
the IMGT exon numbering system and a tyrosine residue at position
96 according to the IMGT exon numbering system (Fc). Then, the
second site may reside on a heavy chain that has a CH3 domain
containing an arginine residue at position 95 according to the IMGT
exon numbering system and a phenylalanine residue at position 96
according to the IMGT exon numbering system (Fc*). In this case,
the CSCP may be an antigen-binding protein described in a preceding
aspect, such as an ScFv fusion protein containing the amino acid
sequences of SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID
NO:30, and SEQ ID NO:31; which in a specific embodiment comprises
SEQ ID NO:19. Here also, the detection molecule (DM) may comprise a
labeled recombinant antigen-binding protein described in a
preceding aspect, such as an antibody or ScFv molecule containing
the amino acid sequences of SEQ ID NO:32, SEQ ID NO:33, SEQ ID
NO:34, SEQ ID NO:35, SEQ ID NO:36, and SEQ ID NO:37; which in a
specific embodiment comprises either SEQ ID NO:40 and SEQ ID NO:41
(anti-Fc* antibody), or SEQ ID NO:43 (ScFv*). Here, the blocking
molecule may be an Fc polypeptide (e.g., single chain), such as
hFc, or any molecule that can bind to the CSCP without also binding
to the DM. In one embodiment, the detection molecule may be a
labeled anti-human IgG F(ab').sub.2.
[0062] In other cases in which the POI is a bispecific antibody,
the first site may reside on a heavy chain that has a CH3 domain
containing an arginine residue at position 95 according to the IMGT
exon numbering system and a phenylalanine residue at position 96
according to the IMGT exon numbering system (Fc*). Then, the second
site may reside on a heavy chain that has a CH3 domain containing a
histidine residue at position 95 according to the IMGT exon
numbering system and a tyrosine residue at position 96 according to
the IMGT exon numbering system. In this case, the CSCP may be an
antigen-binding protein described in a preceding aspect, such as an
ScFv fusion protein containing the amino acid sequences of SEQ ID
NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, and
SEQ ID NO:37; which in a specific embodiment comprises SEQ ID
NO:43. Here also, the detection molecule (DM) may comprise a
labeled recombinant antigen-binding protein described in a
preceding aspect, such as an antibody or ScFv molecule containing
the amino acid sequences of SEQ ID NO:27, SEQ ID NO:28, SEQ ID
NO:29, SEQ ID NO:30, and SEQ ID NO:31; which in a specific
embodiment comprises either a heavy chain and a light chain
(anti-hFc antibody), or SEQ ID NO:19 (ScFv). Here, the blocking
molecule may be an Fc* polypeptide (e.g., single chain), or any
molecule that can bind to the CSCP without also binding to the DM.
In one embodiment, the detection molecule may be a labeled
anti-human IgG F(ab').sub.2.
[0063] In some aspects, the invention provides a method of
detecting or isolating a cell that stably expresses a heterodimeric
protein comprising the steps of (a) expressing in a host cell a
cell surface capture protein (CSCP) and a heterodimeric protein,
wherein (i) the CSCP binds to a first site on the heterodimeric
protein to form a CSCP-heterodimeric protein complex inside the
host cell, (ii) the CSCP-heterodimeric protein complex is
transported through the host cell, and (iii) then displayed on the
surface of the host cell; (b) contacting the host cell with a
detection molecule, wherein the detection molecule binds to a
second site on the heterodimeric protein; and (c) selecting the
host cell which binds the detection molecule. In some embodiments,
the heterodimeric protein comprises multiple subunits and the first
site on the heterodimeric protein resides on a first subunit, and
the second site resides on the heterodimeric protein resides on a
second subunit. In some embodiments, the cell surface capture
molecule comprises an antigen, Protein A, or ScFv capable of
binding the first subunit and not the second subunit.
[0064] In one aspect, the invention provides a method of producing
a bispecific antibody comprising the step of expressing in a host
cell a cell surface capture protein ("CSCP"), an antibody light
chain, a first antibody heavy chain, which contains a CH3 domain
comprising a histidine at IMGT position 95 and a tyrosine at IMGT
position 96, and a second antibody heavy chain, which contains a
CH3 domain comprising an arginine at IMGT position 95 and a
phenylalanine at IMGT position 96. While inside the host cell, the
CSCP binds to the first antibody heavy chain but does not bind to
the second antibody heavy chain, the second antibody heavy chain
binds to the first antibody heavy chain, and the light chains bind
to the heavy chains, thus forming a CSCP-Antibody ternary complex.
This ternary complex is secreted and presented onto the surface of
the host cell. The host cell may be contacted with a blocking
molecule, which binds to a CSCP on the cell surface, but only in
those situations in which the CSCP is not bound to the
antibody-of-interest, i.e., an "empty" CSCP. The host cell is then
contacted with a DM that binds to or is capable of binding to the
second antibody heavy chain. The host cell that binds the DM is
identified, selected, and/or pooled. In some embodiments, the host
cells that bind the DM are selected, pooled, cultured and expanded,
and then subjected to another round of expression, detection,
selection, pooling and expansion. This process may be reiterated
multiple times to enrich for the production of high titers of
bispecific antibodies.
[0065] In one embodiment, the CSCP employed in the method is an
ScFv-fusion protein containing the amino acid sequences of SEQ ID
NO:27, SEQ ID NO:28, SEQ ID NO:29, SEQ ID NO:30, and SEQ ID NO:31.
In one embodiment, the CSCP comprises the amino acid sequence of
SEQ ID NO:19. In one embodiment, the DM employed in the method is a
protein containing the amino acid sequences of SEQ ID NO:32, SEQ ID
NO:33, SEQ ID NO:34, SEQ ID NO:35, SEQ ID NO:36, and SEQ ID NO:37.
In one embodiment, the DM is an antibody comprising a heavy chain
sequence of SEQ ID NO:40 and a light chain sequence of SEQ ID
NO:41. In another embodiment, the DM is an ScFv fusion protein
containing the amino acid sequence of SEQ ID NO:43. A label, for
example a fluorescent moiety like FITC or Alexa Fluor.RTM. 488, may
be attached to the DM. Fluorescence activated cell sorting may be
used as the detection and selection means.
[0066] In an alternative embodiment, the method of producing a
bispecific antibody comprises the step of expressing in a host cell
a cell surface capture protein ("CSCP"), an antibody light chain, a
first antibody heavy chain, which contains a CH3 domain comprising
an arginine at IMGT position 95 and a phenylalanine at IMGT
position 96 (Fc*), and a second antibody heavy chain, which
contains a CH3 domain comprising a histidine at IMGT position 95
and a tyrosine at IMGT position 96. While inside the host cell, the
CSCP binds to the first antibody heavy chain but does not bind to
the second antibody heavy chain, the second antibody heavy chain
binds to the first antibody heavy chain, and the light chains bind
to the heavy chains, thus forming a CSCP-Antibody ternary complex.
This ternary complex is secreted and presented onto the surface of
the host cell. The host cell may be contacted with a blocking
molecule, which binds to a CSCP on the cell surface, but only in
those situations in which the CSCP is not bound to the
antibody-of-interest, i.e., an "empty" CSCP. The host cell is then
contacted with a DM that binds to or is capable of binding to the
second antibody heavy chain. The host cell that binds the DM is
identified, selected, and/or pooled. In some embodiments, the host
cells that bind the DM are selected, pooled, cultured and expanded,
and then subjected to another round of expression, detection,
selection, pooling and expansion. This process may be reiterated
multiple times to enrich for the production of high titers of
bispecific antibodies.
[0067] In one embodiment of this alternative embodiment, the CSCP
employed in the method is an ScFv-fusion protein containing the
amino acid sequences of SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34,
SEQ ID NO:35, SEQ ID NO:36, and SEQ ID NO:37. In one embodiment,
the CSCP comprises the amino acid sequence of SEQ ID NO:43. In one
embodiment, the DM employed in the method is a protein containing
the amino acid sequences of SEQ ID NO:27, SEQ ID NO:28, SEQ ID
NO:29, SEQ ID NO:30, and SEQ ID NO:31. In one embodiment, the DM is
an antibody comprising a heavy chain sequence and a light chain
sequence. In another embodiment, the DM is an ScFv fusion protein
containing the amino acid sequence of SEQ ID NO:19. A label, for
example a fluorescent moiety like FITC or Alexa Fluor.RTM. 488, may
be attached to the DM. Fluorescence activated cell sorting may be
used as the detection and selection means.
[0068] In both the first embodiment and the alternative embodiment,
the host cell, which is the product of the iterative selection,
pooling and expansion, is capable of producing, or does produce
bispecific antibody at a titer of at least 2 g/L, wherein the
bispecific antibody species (Fc/Fc*) represents at least 40% by
mass of the total antibody produced by the host cell
(Fc/Fc+Fc*/Fc*+Fc/Fc*).
[0069] Other objects and advantages will become apparent from a
review of the ensuing detailed description.
DETAILED DESCRIPTION
[0070] Before the present methods are described, it is to be
understood that this invention is not limited to particular
methods, and experimental conditions described, as such methods and
conditions may vary. It is also to be understood that the
terminology used herein is for the purpose of describing particular
embodiments only, and is not intended to be limiting, since the
scope of the present invention will be limited only by the appended
claims.
[0071] As used in this specification and the appended claims, the
singular forms "a", "an", and "the" include plural references
unless the context clearly dictates otherwise. Thus for example, a
reference to "a method" includes one or more methods, and/or steps
of the type described herein and/or which will become apparent to
those persons skilled in the art upon reading this disclosure and
so forth.
[0072] Unless defined otherwise, all technical and scientific terms
used herein have the same meaning as commonly understood by one of
ordinary skill in the art to which this invention belongs. Although
any methods and materials similar or equivalent to those described
herein can be used in the practice or testing of the present
invention, the preferred methods and materials are now described.
All publications mentioned herein are incorporated herein by
reference in their entirety.
[0073] General Description
[0074] The method of the invention provides substantial advantages
over current methods for isolation and identification of
protein-secreting cells. For example, cells that secrete antibodies
may be rapidly and conveniently isolated based on desired
specificity, avidity, or isotype. Furthermore, the amount of
secreted protein produced may be directly quantified, unlike many
methods in the prior art wherein production of secreted protein is
indirectly quantified.
[0075] Recently, two additional methods that utilize flow cytometry
have been developed for the high throughput isolation of stable
high expression cell lines. The first method involves modification
of the expression plasmid to include a transcriptional read out for
the GOI mRNA. This is most often accomplished by inserting an
internal ribosomal entry site (IRES) and a gene whose protein
product is easily monitored by flow cytometry, most frequently
green fluorescent protein (GFP), between the stop codon of the GOI
and the terminal poly A site (Meng et al. (2000) Gene 242:201). The
presence of an IRES allows the POI and GFP to be translated from
the same mRNA. Therefore, the expression level of the GFP gene is
indirectly related to the mRNA level for the GOI. Clones that
accumulate the GFP at high levels are isolated by flow cytometry
and then screened for POI production. Because this method depends
on the coupling of GOI expression to the reporter gene by use of an
IRES in a recombinant construction, it is not applicable to the
isolation of hybridomas.
[0076] The use of flow cytometry in the isolation of expression
clones allows for the rapid analysis of large numbers of clones in
a high throughput format. Moreover, use of flow cytometry
significantly reduces the direct handling of cells. Unfortunately,
the level of GFP production is not a direct measure of the
production level of the POI. Various mechanisms may uncouple the
production of secreted POI from accumulation of GFP. Differences in
production of the POI and the GFP reporter may result from
differences in the translation efficiency of the two genes,
secretion efficiency of the POI, or stability of the polycistronic
mRNA.
[0077] Another method that uses flow cytometry to isolate
expression clones involves encapsulation of cells within agarose
microdrops (Weaver et al. (1990) Methods Enzymol. 2:234). In this
method biotinylated antibodies specific for the POI are bound to
the biotinylated agarose through streptavidin such that secreted
POI is captured and retained within the microdrop (Gray et al.,
(1995) J. Immunol. Methods 182:155). The trapped POI is detected by
immuno-staining with an antibody specific for the POI. To reduce
the encapsulating agarose from absorbing POI secreted from adjacent
cells, the cells are placed in a low-permeability medium. Those
cells with the highest antibody staining of the POI in the
embedding agarose are identified and isolated by flow cytometry.
The gel microdrop approach screens cells directly for their ability
to secrete POI, rather than indirectly screening for expression of
GOI mRNA, but requires the availability of suitable antibodies for
trapping and staining the secreted POI and the procedure requires
special equipment to generate the agarose gel microdrops. Moreover,
some cells may be sensitive to the encapsulation process.
[0078] A variation of this method circumvents the requirement for
embedding cells in a matrix by directly binding an antibody,
specific for the POI, to the cell surface (Manz et al. (1995) PNAS
92:1921-1925). In this method, non-specific biotinylation of cell
surface proteins with biotin-hydroxysuccinimide ester is followed
by contact with a streptavidin-conjugated antibody capable of
binding the POI. Cells secreting the POI become decorated with the
POI which is then detected with an appropriately labeled second
antibody. However, diffusion of POI between neighboring cells is
problematic, and this method also requires a high viscosity medium
to reduce diffusion of POI away from expressing cells. Because
these high viscosity media are required for discriminating cells,
the cells must be washed and placed in a medium suitable for cell
sorting if so desired.
[0079] The problems associated with identification and isolation of
high expression recombinant cell lines especially applies to the
isolation of hybridomas that express an antibody of interest.
However, the identification of useful hybridomas includes several
additional problems; they must be screened first for
antigen-binding activity, then for immunoglobulin isotype.
Moreover, GFP-based methods are not applicable to the
identification and isolation of hybridomas because construction of
hybridomas does not include a recombinant construct such that
expression of the antibody genes can be linked to a transcriptional
reporter such as GFP. Hybridoma screening is a slow, laborious
endeavor where the number of clones screened is limited by existing
technologies.
[0080] The instant invention describes a novel and previously
unknown method of identifying and isolating cells that produce
secreted proteins. The invention is based on the production of a
cell line that expresses a molecule, localized to the cell surface,
which binds the POI. The cell surface-displayed POI can then be
detected by labeling with various detection molecules. The amount
of POI displayed on the cell surface, under specific conditions, is
a direct measure of the total amount of POI secreted. POI producers
may then be isolated from non-producers, and levels of production
or POI characteristics may be differentiated. The advantage of the
invention is that it directly quantifies the secreted POI rather
than indirectly measuring the mRNA.
[0081] This invention relates to the construction or use of cells
that express cell surface capture molecules which bind various
secreted POIs in the same cell that produces the POI. As the cell
secretes the POI, these cell surface capture molecules bind it, or
complexes of POI and cell surface capture molecules may form
intracellularly and then get secreted. Binding may occur in an
autocrine manner or while being secreted. The cells that produce
the secreted POI may then be identified and isolated. Such
identification and isolation may be based on characteristics of the
POI, production of the POI or lack thereof, or by specified levels
of production. The cell surface capture molecule and/or the POI may
be produced by the cell in its native state, or the cell surface
capture molecules and/or the POI may be recombinantly produced.
Through the construction or use of such a cell, any secreted
protein may be captured by the cell surface capture molecule
provided there is a corresponding affinity between the two. As
explained further, any molecule may be manipulated such that it can
be used as a cell surface capture molecule. Therefore, this
invention may be utilized to isolate any cell that secretes a
protein.
[0082] Most any protein has the capacity to function as a cell
surface capture molecule as described by the invention. What is
necessary is the ability of the desired protein to be anchored to
the cell membrane and exposed to the extracellular space. If the
desired cell has a signal sequence then only a membrane anchor,
including but not limited to a transmembrane anchor or a GPI
linkage signal, need be added to the cell surface capture molecule
such that it remains anchored in the cell membrane exposed to the
outside of the cell. Furthermore, if the desired protein lacks a
signal sequence, a signal sequence may be added to the amino
terminus of the desired protein, such that it is transported to the
cell surface. A signal sequence and a membrane anchor may be native
to the cell, recombinant, or synthetic.
[0083] Cells often secrete a wide variety of proteins, endogenously
or following the introduction of recombinant DNA. Any secreted
protein may be identified and the cell producing it may be isolated
according to the method of this invention. Such secreted proteins
include but are not limited to growth factors, growth factor
receptors, ligands, soluble receptor components, antibodies,
bispecific antibodies, recombinant Trap molecules, Fc-containing
fusion proteins, sTCRs, TCR-Fc's, and peptide hormones. Such
secreted proteins may or may not be recombinant. That is, the
secretion of some proteins of interest from the desired cell may
not require the introduction of additional nucleotide sequences.
For example, the secretion of antibodies from B-cells or plasma
cells is not the result of introduction of recombinant nucleotide
sequences into the B-cell or plasma cell. Recombinant secreted
proteins may be produced by standard molecular biology techniques
well known to the skilled artisan (see e.g., Sambrook, J., E. F.
Fritsch And T. Maniatis. Molecular Cloning: A Laboratory Manual,
Second Edition, Vols 1, 2, and 3, 1989; Current Protocols in
Molecular Biology, Eds. Ausubel et al., Greene Publ. Assoc., Wiley
Interscience, NY). These secreted proteins are useful for many
commercial and research purposes. This invention encompasses the
production of such secreted proteins through the methodologies of
the invention. Detection of the cells with the displayed POI may be
accomplished through the use of any molecule capable of directly or
indirectly binding the displayed POI. Such detection molecules may
facilitate the detection and/or isolation of the cells displaying
the POI.
[0084] The invention is applicable to the isolation of, inter alia,
a) ligand-producing cells by using the ligand-specific receptor as
the cell surface capture molecule, b) soluble receptor-producing
cells by using a surface bound receptor-specific ligand as the cell
surface capture molecule, c) antibody-producing cells by using an
antibody-binding protein as the cell surface capture molecule, d)
sTCR's by using an s-TCR-binding protein (e.g., and antigen
recognized by the TCR) as the cell surface capture molecule, e)
TCR-Fc's, by using an Fc-binding protein as a cell surface capture
molecule, or f) bispecific antibodies that harbor a mutation in one
of its CH3 domains that abrogates protein A binding, by using a
fusion protein capture molecule that comprises an ScFv domain fused
to an Fc.gamma.R transmembrane and cytoplasmic domain.
[0085] In accordance with the methodology of this invention, a cell
is first transfected with a vector containing a nucleotide sequence
that encodes a cell surface capture molecule that is capable of
binding the secreted POI, under conditions in which such cell
surface capture molecule is expressed. Transfected cells which are
appropriate producers of such cell surface capture molecules are
then detected and isolated, and such cells are cultured. These
cells may either naturally produce the POI, or the POI may be
recombinantly produced. If the cells naturally produce the POI,
they are ready for detection and isolation. If the POI is to be
recombinantly produced, then the isolated and cultured cells
expressing the specified cell surface capture molecule are
transfected with second nucleotide sequence that encodes the
secreted POI, under conditions in which the secreted POI is
expressed. Upon expression, the secreted POI binds to the cell
surface capture molecules and the cells displaying bound POI are
detected and isolated.
[0086] If the POI is naturally produced by the cell, the cell will
not be transfected with nucleotide sequence encoding the POI.
Therefore, this aspect of the invention is applicable to any and
all cells producing a POI. In addition, if the cell surface capture
molecule is naturally produced by the cell, the cell need not be
transfected with nucleotide sequences encoding the cell surface
capture molecule. Therefore, this aspect of the invention is
applicable to any and all cells producing a cell surface capture
molecule.
[0087] A wide variety of host cells may be transfected. These cells
may be either of eukaryotic or of prokaryotic origin. The cells
will often be immortalized eukaryotic cells, and in particular,
mammalian cells, for example monkey kidney cells (COS), Chinese
hamster ovary cells (CHO), HeLa cells, baby hamster kidney cells
(BHK), human embryonic kidney cells (HEK293), leukocytes, myelomas,
cell lines transfected with adenovirus genes, for example, AD5 E1,
including but not limited to immortalized human retinal cells
transfected with an adenovirus gene, for example, PER.C6.TM. cells,
and embryonic stem cells. The cells may also be non mammalian cells
including bacterial, fungi, yeast and insect cells, including, but
not limited to, for example Escherichia coli, Bacillus subtilus,
Aspergillus species, Saccharomyces cerevisiae, and Pichia pastoris.
All cells may be grown in culture trays medium under appropriate
conditions or in a synergistic host. The most desirable cells will
be mammalian cells capable of culture.
[0088] The secreted POI bound to the cell surface capture molecule
may be detected and isolated by various techniques known in the
art. Cultures cells displaying the secreted POI may be contacted
with (a) molecule(s) capable of directly or indirectly binding the
secreted POI wherein such detection molecule(s) may contain a
detection label, such as, for example, a chromogenic, fluorogenic,
colored, fluorescent, or magnetic label. The label bound to the
detection molecule may be detected and the cell isolated using
various methods. Most preferably, within a cell population the
label will be detected and the cell isolated utilizing flow
cytometry. Alternatively, the detection molecule may be used for
the direct isolation of cells displaying the POI. This may be
accomplished by conjugation of the detection molecule to a culture
plate, paramagnetic molecules, or any other particle or solid
support. In addition, displayed POI may be detected directly by a
property of the detection molecule or the POI.
[0089] In one embodiment, two detection molecules that bind each
other and are differentially labeled are used to detect a displayed
secreted POI that blocks that interaction. If a cell displays a
secreted POI that binds the first detection molecule and blocks the
interaction between the first and second detection molecule, that
cell may be isolated based on the presence of only the first
detection molecule on its surface. On the other hand, if a cell
displays a secreted POI that binds the first detection molecule but
does not block the interaction between the first and second
detection molecule, that cell may be isolated based on the presence
of both detection molecules on its surface. For example, antibody
producing cells expressing antibodies that specifically block, or
do not block, the formation of a receptor-ligand complex may be
identified. If the detection molecules are a receptor and its
ligand which are differentially labeled, then an antibody producing
cell that expresses antibodies that block the receptor-ligand
complex from forming may be detected by the presence of one label
on its surface, whereas an antibody producing cell that expresses
antibodies that do not block the receptor-ligand complex from
forming may be detected by the presence of both labels on its
surface.
[0090] In any of the embodiments and with regards to isolating
expressing cells from non-expressing cells or lesser expressing
cells, one of the principal difficulties, when the POI is a
secreted protein, is diffusion of POI between neighboring cells.
Therefore, it is critical that any system that is designed to
capture the secreted POI on the cell surface must prevent the
diffusion of the POI from the expressing cell to a neighboring cell
and its adherence to that cell. If diffusion is allowed to occur,
and neighboring cells become decorated with the secreted POI, then
separation of cells based upon the degree of POI decoration will
fail to discriminate high expressing cells from cells with low
expression levels, and may fail to effectively isolate expressing
from non-expressing cells.
[0091] Therefore one embodiment of this invention is to block the
diffusion of the secreted POI between neighboring cells. This may
be accomplished by the addition of a blocking molecule that binds
either the cell surface capture molecule or the POI and prevents
the binding of the secreted POI to the cell surface capture
molecule. In this aspect, the detection molecules do not bind the
blocking molecule. For example, if the cell surface receptor is the
hFc.gamma.RI and the secreted POI possesses the human IgG Fc
fragment, then diffusion of the secreted POI between neighboring
cells may be blocked by the addition of exogenous rat IgG to the
culture media. Detection of cells displaying secreted POI, and not
bound rat IgG, is achieved by use of antibodies specific for human
IgG Fc that do not recognize rat IgG. In another embodiment,
binding of the secreted POI between neighboring cells is reduced by
increasing the viscosity of the media.
[0092] In one embodiment of this invention, the secreted POI is not
allowed to accumulate in the media. This may be accomplished by
regulating the expression of the secreted POI and/or the cell
surface capture molecule such that brief expression of the POI
results in sufficient POI to bind the cell surface capture molecule
but insufficient amounts for diffusion. In another embodiment,
cells may be removed from the media containing accumulated POI, the
POI bound to the cells is stripped off, and POI expression is
allowed to continue for a limited period of time such that secreted
POI does not accumulate in the media. Proteins may be stripped by
methods known in the art, for example, washing cells with low pH
buffer.
[0093] According to this invention, those cells in a cell
population that bind the most detection molecules also express the
most secreted POI. In fact, the more POI that an individual cell
secretes, the more POI is displayed on the cell surface. This
correlation between the amount of surface-displayed POI and the
expression level of the POI in that cell allows one to rapidly
identify cells with a desired relative expression level from a
population of cells.
[0094] In one embodiment, a DNA library may be used to express
secreted protein which may be displayed on the cell surface by the
cell surface capture molecule. For example, a library of DNA may
also be generated from the coding regions of the antibody variable
domains from B-cells isolated from immunized animals. The DNA
library may then be expressed in a cell that expresses a cell
surface capture molecule specific for antibodies such that clones
of desired specificity, isotype, or avidity may be identified and
isolated by the method of the invention. In another embodiment, a
library of DNA may be generated from the coding regions of T cell
receptor variable domains from T-cells, and fused to, for example,
an Fc capable of binding to an Fc-binding protein. The DNA library
may them be expressed in a cell that expresses an Fc-binding
protein such that clones of desired specificity, isotype, or
avidity may be identified and isolated as described herein.
[0095] In another embodiment, transgenic mammals may be created
that express a particular cell surface capture molecule in one or
more cell types. The cells from such transgenic mammals may then be
screened directly for the production of a POI. For example, it may
be desirable to express a cell surface capture molecule, specific
for antibodies, in plasma cells. Accordingly, plasma cells from
immunized mice may be harvested and those cells producing
antibodies specific to the desired antigen may be isolated by the
method of the invention.
[0096] In a further embodiment of the invention, antibody
production is measured through the use of a CHO cell line that
expresses the human Fc.gamma.R1 receptor (Fc.gamma.RI) which binds
the particular antibody or TCR-Fc that is the POI.
[0097] In another aspect of the invention, the protein of interest
comprises one or more T cell receptor variable domains or a soluble
T cell receptor. The one or more T cell receptor variable domains
can be covalently linked to a moiety that can bind a cell surface
capture protein. In a specific embodiment, the one or more T cell
receptor variable domains are fused to an Fc sequence, e.g., a
human Fc sequence, and the cell surface capture protein is an Fc
receptor, e.g., an Fc.gamma.R.
[0098] The general structures of TCR variable domains are known
(see, e.g., Lefranc and Lefranc (2001) The T Cell Receptor
FactsBook, Academic Press, incorporated herein by reference; see,
e.g., pp. 17-20; see also, Lefranc et al. (2003) IMGT unique
numbering for immunoglobulin and T cell receptor variable domains
and Ig superfamily V-like domains, Developmental and Comparative
Immunology 27:55-77, and Lefranc et al. (2005) IMGT unique
numbering for immunoglobulin and T cell receptor constant domains
and Ig superfamily C-like domains, Developmental and Comparative
Immunology 29:185-203, each incorporated herein by reference). In
one embodiment, a TCR variable domain of a TCR-Fc comprises an
N-terminal region having a variable domain of 104-125 amino acids.
In another embodiment, the TCR-Fc further comprises a TCR constant
region comprising 91-129 amino acids. In another embodiment, the
TCR-Fc further comprises a connecting peptide comprising 21-62
amino acids.
[0099] In one embodiment, the Fc sequence is fused directly or
through a linker to the TCR variable domain. In another embodiment,
the TCR-Fc comprises a TCR variable region and a TCR constant
region, and the Fc sequence is fused directly or through a linker
to the TCR constant region. In another embodiment, the TCR-Fc
comprises a TCR variable region, a TCR constant region, and a
connecting peptide, and the Fc sequence is fused directly or
through a linker to the connecting peptide.
[0100] The sTCR, TCR-Fc, or fusion protein comprising one or more T
cell receptor variable regions can be selected so as to
specifically bind an antigen of interest, for example, a substance
produced by a tumor cell, for example, tumor cell substance that is
capable of producing an immune response in a host. In a specific
embodiment, the antigen is an antigen that is present on the
surface of a tumor cell (i.e., a tumor antigen), is recognized by a
T cell, and that produces an immune response in a host. Tumor
antigens include, for example, alphafetoprotein (AFP),
carcinoembryonic antigen (CEA), MUC-1, epithelial tumor antigen
(ETA), tyrosinase (e.g., for malignant melanoma),
melanoma-associated antigen (MAGE), and mutated or abnormal forms
of other proteins such as, for example, ras, p53, etc.
[0101] In one embodiment, the POI is a TCR-Fc, and the TCR-Fc
comprises a TCR .alpha. chain variable region fused to an Fc
sequence and a TCR .beta. chain fused to the Fc sequence (each
directly or through a linker), wherein the TCR .alpha. chain-Fc
fusion and the TCR .beta. chain-Fc fusion associate to form an
.alpha..beta. TCR-Fc. In a specific embodiment, the .alpha..beta.
TCR-Fc comprises the following two polypeptides: (1) a TCR .alpha.
chain variable region fused to a TCR .alpha. chain constant region
fused to an Fc sequence, and (2) a TCR .beta. chain variable region
fused to a TCR .beta. chain constant region fused to an Fc
sequence.
[0102] In another embodiment, the POI is a TCR-Fc having a TCR
.alpha. variable region and a TCR .beta. variable region and,
optionally, a TCR .alpha. constant region and/or a TCR .beta.
constant region. In a specific embodiment, the TCR-Fc is encoded by
a nucleic acid comprising (5' to 3') a TCR .alpha. variable region
sequence, optionally followed by a TCR .alpha. constant region
sequence, a TCR .beta. variable region sequence, optionally
followed by a TCR .beta. constant region sequence, optionally a
linker, then an Fc sequence. In a specific embodiment, the TCR-Fc
is encoded by a nucleic acid comprising (5' to 3') a TCR .beta.
variable region sequence, optionally followed by a TCR .beta.
constant region sequence, a TCR .alpha. variable region sequence,
optionally followed by a TCR .alpha. constant region sequence,
optionally a linker, then an Fc sequence. In various embodiments,
constructs encoding TCR-Fc's are preceded by signal sequences,
e.g., secretion signal sequences, to render them secretable.
[0103] In another embodiment, the POI is a TCR-Fc, and the TCR-Fc
comprises a TCR-Fc comprising a TCR .gamma. chain fused to an Fc
sequence and a TCR .delta. chain variable region fused to an Fc
sequence to form a .gamma..delta. TCR-Fc. In a specific embodiment,
the .gamma..delta. TCR-Fc comprises the following two polypeptides:
a TCR .gamma. chain variable region fused to a TCR .gamma. chain
constant region fused to an Fc sequence, and (2) a TCR .delta.
chain variable region fused to a TCR .delta. chain constant region
fused to an Fc sequence.
[0104] T cell receptor variable regions can be identified and/or
cloned by any method known in the art. The T cell receptor variable
regions of the protein of interest are obtainable, for example, by
expressing rearranged T cell receptor variable region DNA in a
cell, for example, fused to a human Fc sequence. Rearranged T cell
receptor variable regions specific for a particular antigen can be
obtained by any suitable method known in the art (see references
below), for example, by exposing a mouse to an antigen and
isolating T cells of the mouse, making hybridomas of the T cells of
the mouse, and screening the hybridomas with the antigen of
interest to obtain a hybridoma of interest. Rearranged T cell
variable regions specific for the antigen of interest can be cloned
from the hybridoma(s) of interest. T cell receptor variable regions
specific for an antigen can also be identified using phage display
technology, for example, as provided in references below. The
variable regions can then be cloned and fused, for example, to a
human Fc to make a protein of interest that can bind to a cell
surface capture molecule that is an Fc.gamma.R.
[0105] Methods for identifying and/or cloning T cell receptor
variable regions are described, for example, in U.S. Pat. No.
5,635,354 (primers and cloning methods); Genevee et al. (1992) An
experimentally validated panel of subfamily-specific
oligonucleotide primers (V.alpha.1-w29A/V.beta.1-w24) for the study
of human T cell receptor variable V gene segment usage by
polymerase chain reaction, Eur. J. Immunol. 22:1261-1269 (primers
and cloning methods); Gorski et al. (1994) Circulating T Cell
Repertoire Complexity in Normal Individuals and Bone Marrow
Recipients Analyzed by CDR3 Size Spectratyping, J. Immunol.
152:5109-5119 (primers and cloning methods); Johnston, S. et al.
(1995) A novel method for sequencing members of multi-gene
families, Nucleic Acids Res. 23/15:3074-3075 (primers and cloning
methods); Pannetier et al. (1995) T-cell repertoire diversity and
clonal expansions in normal and clinical samples, Immunology Today
16/4:176-181 (cloning methods); Hinz, T. and Kabelitz, D. (2000)
Identification of the T-cell receptor alpha variable (TRAV) gene(s)
in T-cell malignancies, J. Immunol. Methods 246:145-148 (cloning
methods); van Dongen et al. (2002) Design and standardization of
PCR primers and protocols for detection of clonal immunoglobulin
and T-cell receptor gene recombinations in suspect
lymphoproliferations: U.S. Pat. No. 6,623,957 (cloning methods and
primers); Report of the BIOMED-2 Concerted Action BMH4-CT98-3936,
Leukemia 17:2257-2317 (primers and cloning methods); Hodges et al.
(2002) Diagnostic role of tests for T cell receptor (TCR) genes, J.
Clin. Pathol. 56:1-11 (cloning methods); Moysey, R. et al. (2004)
Amplification and one-step expression cloning of human T cell
receptor genes, Anal. Biochem. 326:284-286 (cloning methods);
Fernandes et al. (2005) Simplified Fluorescent Multiplex PCR Method
for Evaluation of the T-Cell Receptor V.beta.-Chain Repertoire,
Clin. Diag. Lab. Immunol. 12/4:477-483 (primers and cloning
methods); Li, Y. et al. (2005) Directed evolution of human T-cell
receptors with picomolar affinities by phage display, Nature
Biotech. 23/3:349-354 (primers and cloning methods); Wlodarski et
al. (2005) Pathologic clonal cytotoxic T-cell responses: nonrandom
nature of the T-cell receptor restriction in large granular
lymphocyte leukemia, Blood 106/8:2769-2780 (cloning methods);
Wlodarski et al. (2006) Molecular strategies for detection and
quantitation of clonal cytotoxic T-cell responses in aplastic
anemia and myelodysplastic syndrome, Blood 108/8:2632-2641 (primers
and cloning methods); Boria et al. (2008) Primer sets for cloning
the human repertoire of T cell Receptor Variable regions, BMC
Immunology 9:50 (primers and cloning methods); Richman, S. and
Kranz, D. (2007) Display, engineering, and applications of
antigen-specific T cell receptors, Biomolecular Engineering
24:361-373 (cloning methods). Examples of sTCRs are provided in,
for example, U.S. Pat. Nos. 6,080,840 and 7,329,731; and, Laugel, B
et al. (2005) Design of Soluble Recombinant T Cell Receptors for
Antigen Targeting and T Cell Inhibition, J. Biol. Chem.
280:1882-1892; incorporated herein by reference. Fc sequences are
disclosed herein; examples of Fc sequences, and their use in fusion
proteins, are provided, for example, in U.S. Pat. No. 6,927,044 to
Stahl et al. All of the foregoing references are incorporated
herein by reference.
[0106] In a further embodiment of the invention, the cell surface
capture molecule is designed to engage and display those proteins
of interest that are normally incapable of binding with sufficient
affinity or bind with low affinity to an Fc.gamma.R capture
molecule. Those proteins of interest include IgG4 and IgG2
molecules. Thus, a modular capture molecule was designed and built
based upon an ScFv domain fused to an Fc.gamma.R transmembrane and
cytoplasmic domain. The ScFv domain was derived from a high
affinity anti-humanFc antibody, and contains a heavy chain variable
domain fused to a light chain variable domain. The
Fc.gamma.R-TM-cytoplasmic domain was used to enable the proper
insertion and orientation in the plasma membrane. The
ScFv-Fc.gamma.R-TM-cyto fusion protein is capable of binding IgG4
and other Fc containing molecules, as well as IgG2 and IgG1
subtypes, and those heterodimeric (e.g., bispecific antibodies)
comprising at least one wild type CH3 domain, wherein the other CH3
domain may contain an Fc*-type substitution.
[0107] In a further embodiment of the invention, the cell surface
capture molecule is designed to engage and display those proteins
of interest that contain a modified CH3 domain, such as the Fc*
polypeptide, which comprises H95R and Y96F amino acid substitutions
(the numbering is based upon the IMGT system), e.g., SEQ ID NO: 42.
Those proteins of interest include bispecific antibodies, such as
antibody heterotetramers that are useful in the manufacture of
bispecific antibodies are generally described in US Patent
Application Publication No. US 2010/0331527 A1, Dec. 30, 2010,
which is incorporated in its entirety herein by reference. Thus, a
modular capture molecule was designed and built based upon an ScFv*
domain fused to an Fc.gamma.R transmembrane and cytoplasmic domain.
The ScFv* domain was derived from a high affinity anti-Fc*
antibody, and contains heavy chain variable domain fused to a light
chain variable domain. The Fc.gamma.R-TM-cytoplasmic domain was
used to enable the proper insertion and orientation in the plasma
membrane. The ScFv*-Fc.gamma.R-TM-cyto fusion protein binds any
Fc*-containing molecule, such as wildtype IgG3, and heterodimers of
IgG4, IgG2, and IgG1, which contain at least one Fc* polypeptide
sequence.
EXAMPLES
[0108] The following examples are put forth so as to provide those
of ordinary skill in the art with a complete disclosure and
description of how to make and use the methods and compositions of
the invention, and are not intended to limit the scope of what the
inventors regard as their invention. Efforts have been made to
ensure accuracy with respect to numbers used (e.g., amounts,
temperature, etc.) but some experimental errors and deviations
should be accounted for. Unless indicated otherwise, parts are
parts by weight, molecular weight is average molecular weight,
temperature is in degrees Centigrade, and pressure is at or near
atmospheric.
Example 1
[0109] Construction of pTE084.
[0110] pTE084 was constructed by ligating the 1,436 bp Xba I
fragment from pCAE100 that encodes the human Fc.gamma.RI
(hFc.gamma.RI; GenBank accession number M21091) into the Xba I site
of pRG821. The orientation of hFc.gamma.RI in desirable plasmids
resulting from the ligation was examined by restriction mapping
with Not I, Pst I, Eco RI, and Stu I. pTE084 was designed for the
high level expression of hFc.gamma.RI, the high affinity cell
surface receptor for the Fc domain of human IgG. It contains two
independent expression cassettes. One cassette is a hFc.gamma.RI
gene driven by the CMV-MIE promoter, and the second cassette is the
neomycin phosphotransferase II (npf) gene, which confers resistance
to G418, driven by the SV40 late promoter.
[0111] Construction of a CHO K1 Derivative that Expresses
hFc.gamma.RI.
[0112] CHO K1 cells (4.times.10.sup.6) were transfected with pTE084
using Lipofectamine.TM. (Life Technologies; Rockville, Md.)
following manufacturer's suggestions. The cells were placed in the
culture medium (10% fetal bovine serum, 90% Ham's F-12, 2 mM
L-glutamine; all reagents were from Life Technologies, Rockville,
Md.) containing 500 .mu.g/ml G418 (Life Technologies) for 15 days.
The cells that survived G418 selection were trypsinized, pooled,
and stained with FITC-conjugated human IgG, Fc fragment (FITC-hFc;
Jackson ImmunoResearch Laboratories, West Grove, Pa.). Briefly, the
cells grown on 10 cm culture plates were washed once with
Dulbecco's phosphate-buffered saline (PBS) without calcium chloride
and magnesium chloride (Life Technologies). Three milliliters of
0.25% trypsin (Life Technologies) were added to each plate. The
plates were swirled until the cells detached from the plate. Ten
milliliters of culture medium was immediately added to each plate
of the detached cells. The cells were then collected by
centrifugation at 1,000.times.g for 4 minutes. After removal of
supernatant, the cells were resuspended in 4 ml of 2 .mu.g/ml
FITC-hFc diluted in culture medium. The cells were then placed on a
platform shaker and stained for one hour at room temperature. To
remove unbound FITC-hFc, the cells were washed twice with 20 ml
PBS. The degree of FITC-hFc label on the cells was measured by flow
cytometry on a MOFLO.TM. cell sorter (Cytomation; Fort Collins,
Colo.). The FITC-hFc did not stain mock-transfected parental CHO K1
cells but gave rise to a distribution of fluorescence in the
G418-resistant, pTE084-transfected pool. The top 1% most
fluorescent cells from the selected pool were placed into 96-well
plates at 1 cell/well by flow cytometry. Nine days later, 88 cell
clones in the 96-well plates were expanded into 24-well plates.
After 3 days, the cells in individual wells were washed once with 1
ml PBS, stained with 0.5 ml of 2 .mu.g/ml FITC-hFc for 1 hour,
washed twice with 1 ml PBS and examined for cell surface staining
under a fluorescent microscope. The thirty three most fluorescent
clones were chosen, expanded, then screened by flow cytometry.
[0113] Diffusion of secreted protein between expressing cells and
non-expressing cells among cells was blocked by adding IgG: As all
cells in a hFc.gamma.RI clonal cell line express a cell surface
hFc.gamma.RI, they all possess the ability to bind IgG or fusion
proteins consisting of the Fc domain of IgG. Because hFc.gamma.RI
binds IgG from a variety of species (van de Winkel and Anderson,
1991), a panel of animal IgGs was tested for the ability to block
the binding of a protein containing a human IgG1 (hIgG1) Fc tag
(4SC622) to hFc.gamma.RI-expressing cells. 4SC622 is a chimeric
molecule consisting of IL-2R.gamma. extracellular domain fused to
the hIL-4R.gamma. extracellular domain which is then fused to the
hIgG1-Fc domain. In this experiment, cultures of RGC1, an
hFc.gamma.RI-expressing cell line selected from CHO K1 cells that
have been stably transfected with pTE084, were incubated with 1
.mu.g/ml 4SC622 for 18 hours in the presence or absence of 1 mg/ml
IgG from different species in a 37.degree. C. tissue culture
incubator.
[0114] Cell surface binding of 4SC622 was determined by flow
cytometry after washed cells were stained with
phycoerythrin-conjugated mouse IgG1 monoclonal AG184 (PE-AG184)
specific for the hIL-2R.gamma. component of 4SC622 (BD Pharmingen;
San Diego, Calif.), following procedures outlined for cell staining
with FITC-hFc.
[0115] It was found that hIgG completely blocked 4SC622 from
binding to the hFc.gamma.R1 expressed on the surface of RGC1. Rat,
rabbit and canine-derived IgG also effectively blocked binding
whereas bovine and ovine-derived IgG did not block. The ability of
exogenously added rat IgG to block the binding of an exogenously
added hIgG1 Fc-tagged protein (4SC622) to cell surface hFc.gamma.RI
suggests that rat IgG can also block transfer between cells
expressing a hIgG1 Fc-tagged protein at different levels. To test
this, two cell lines that can be distinguished by the presence or
absence of the green fluorescent protein (EGFP) were generated from
RGC1. Briefly, to mark RGC1 cells with EGFP, 2.times.10.sup.6 RGC1
cells were co-transfected with 0.5 mg PTE073 which encodes a
hygromycin B phosphotransferase gene driven by phosphoglycerate
kinase promoter, and 5 mg pRG816-EGFP which encodes EGFP gene
driven by CMV-MIE promoter. The transfected cells were selected
with 200 .mu.g/ml hygromycin B (Sigma; St. Louis, Mo.) for two
weeks. Green fluorescent cells were isolated by flow cytometry. One
EGFP and hFc.gamma.RI-expressing clone, RGC2, was used in cell
mixing experiments. The other cell line used in these experiments,
RGC4, was generated by stable transfection of RGC1 with plasmid
pEE14.1-622. pEE14.1-622 is a plasmid in which expression of 4SC622
is driven by the CMV-MIE promoter and includes a glutamine
synthetase minigene, which confers resistance to the analog
methionine sulfoximine (MSX), and allows for selection of stable
integration events. RGC4 cells express hFc.gamma.RI on the cell
surface and secrete the hIgG1 Fc-tagged protein 4SC622. One plate
of mixed cells comprising 50% RGC2 and 50% RGC4 cells was incubated
with 1 mg/ml rat IgG for 18 hours prior to staining with PE-AG184
then examined by flow cytometry. EGFP fluorescence of RGC2 cells
shows that RGC2 cells also bind exogenously added 4SC622 (1
.mu.g/ml) as indicated by an increase in PE-AG184 fluorescence.
RGC4 did not fluoresce in the EGFP gate. Significantly, exogenously
added rat IgG did not reduce the percentage of RGC4 cells that
stained positive for cell surface 4SC622, suggesting that the
binding of 4SC622 to hFc.gamma.RI occurred while the proteins were
in transit to the cell surface. When RGC2 and RGC4 cells were
mixed, the 4SC622 protein secreted from RGC4 cells accumulated in
the medium and bound most of the RGC2 cells. However, the addition
of 1 mg/ml rat IgG significantly reduced the percentage of RGC2
cells that bound 4SC622, demonstrating that rat IgG blocked the
transfer of secreted hIgG1 Fc-tagged protein from expressing cells
to non-expressing cells.
Example 2: Cell Surface Fluorescence Correlates with the Expression
Level of 4SC622
[0116] RGC1 cells (4.times.10.sup.6) were transfected with
pEE14.1-622 and a pool of stable transfectants was obtained after
selection for 2 weeks in medium comprised of 10% dialyzed fetal
bovine serum, 90% glutamine-free Dulbecco's Modified Eagle's Medium
(DMEM), 1.times.GS supplement, and 25 .mu.M MSX (All reagents were
from JRH Biosciences, Lenexa, Kans.). Rat IgG was added to the
culture medium to 1 mg/ml 18 hours prior to immunostaining. The
cells were trypsinized, washed with PBS, and stained with 1.5
.mu.g/ml of a polyclonal FITC-conjugated anti-human IgG (H+L)
F(ab')2 fragment (Jackson ImmunoResearch Laboratories) for one hour
at room temperature following procedures as described for FITC-hFc
staining in Example 1. Cell staining was then analyzed by flow
cytometry. The distribution of fluorescence suggested that the
selected pool contained cells with a wide range of 4SC622
expression levels. Cells in the top 3% (R3 bracket), 7-11% (R5
bracket), and 15-19% (R7 bracket) with respect to their
immunofluorescence were sorted into three distinct pools and
expanded for 9 days. Average 4SC622 production per cell for the
pools was determined by measuring cell numbers and 4SC622 levels in
the media after 3 days growth by an immuno-based Pandex assay
(Idexx; Westbrook, Me.) following the manufacturer's
recommendations. In the Pandex assay, fluoricon polystyrene assay
particles coated with goat anti-human IgG, g-chain specific
antibody (Sigma) were used to capture 4SC622 from the medium, and a
FITC-conjugated goat anti-human IgG, Fc specific (Sigma) was used
to detect bead-bound 4SC622. Known amounts of purified 4SC622 were
included in the assay for calibration. Cells in the top 3%, 7-11%,
and 15-19% pool were found to produce 4SC622 at 1.42, 0.36, and
0.22 pg/cell/day, respectively. Thus, there was a correlation
between cell surface 4SC622 staining and specific protein
production. This result suggests that individual cells that express
4SC622 at high levels may be obtained by isolating cells that were
stained brightest by the polyclonal FITC-conjugated anti-human IgG
(H+L) F(ab')2 fragment.
Example 3: Isolation of Expression Clones in RGC1: IL-4 Trap
[0117] To directly demonstrate the efficiency in generating clonal
cell lines with high level secreted protein production by our
methodology, clonal 4SC622 producing cell lines were generated from
RGC1. RGC1 cells (4.times.10.sup.6) were transfected with
pEE14.1-622, and selected for two weeks with 25 .mu.M MSX to obtain
a pool of stable transfectants. MSX-resistant cells were pooled and
incubated with 1 mg/ml human IgG for 18 hours, prior to staining
with PE-AG184. Six cells from the top 5% gate, as determined by
flow cytometry analysis of cell surface 4SC622 staining, were
isolated and expanded. 4SC622 production from the six clonal lines
was determined and compared to 4SC622 production from clones
obtained by hand-picking selected colonies followed by dilution
cloning and amplification. One RGC1-derived clone, RGC4, produced
4SC622 at 12 pg/cell/day. This level is similar to that of the best
4SC622 producer isolated by hand-picking and analyzing 2,700
clones. Thus, compared with hand-picking colonies, the methodology
outlined in this invention proves to be far more efficient in the
screening and cloning of high producers.
[0118] VEGF Trap.
[0119] Plasmids pTE080 and pTE081 encode the genes for VEGF Traps,
hVEGF-R1R2 and hVEGF-R1R3. hVEGF-R1R2 is a chimeric molecule
consisting of the first Ig domain of hVEGFR1 fused to the second Ig
domain of hVEGFR2 which is then fused to the hIg1Fc domain.
hVEGF-R1R3 is a chimeric molecule consisting of the first Ig domain
of hVEGFR1 fused to the second Ig domain of hVEGFR3 which is then
fused to the hIgG1-Fc domain. In these plasmids, the gene for the
VEGF Trap is driven by the CMV-MIE promoter and a glutamine
synthetase minigene, which confers resistance to MSX, is expressed
for selection of stable integration events. RGC1 cells were
transfected with either of these plasmids and grown in medium
containing 25 .mu.M MSX for 2 weeks to select for cells in which
the plasmid has stably integrated. MSX-resistant cells were
incubated with 0.1 .mu.g/ml IgG2a and mouse IgG3 for 18 hours prior
to staining with 1.5 .mu.g/ml polyclonal FITC-conjugated anti-human
IgG (H+L) F(ab')2 fragment. Cell were stained for 1 hour then
washed twice with PBS prior to flow cytometry. Single cells were
sorted into 96-well tissue culture plates from the pool of cells
whose fluorescence was among the highest 1%. The cells in
individual wells were expanded and their productivities were
determined by Pandex assays. RGC-derived clones expressing both
hVEGF-R1R2 and hVEGF-R1R3 had higher specific productivities and
were isolated by screening fewer clones as compared to the
highest-expressing hand-picked MSX-resistant colonies. See Table
1.
TABLE-US-00001 TABLE I SPECIFIC PRODUCTIVITY COMPARISON Hand-picked
CHO K1 RGC1-derived Tran- Stable Cell Lines Stable Cell Lines sient
Sp. Prod. # clones Sp. Prod. # clones Protein (.mu.g/ml)
(pg/cell/day) screened (pg/cell/day) screened 4SC622 1.1 12 2700 12
6 hVEGF- 33 68 190 77 62 R1R2 hVEGF- 27 5 100 22.6 42 R1R3
Example 4: Cell Surface-Bound hIgG1 Fc-Tagged Protein is
Internalized by RGC1
[0120] hFc.gamma.RI is known to induce internalization of its cell
surface-bound ligand. To analyze whether RGC1 cells could
internalize cell surface-bound 4SC622, 1 .mu.g/ml 4SC622 was added
to RGC1 cells for 1 hour and then the cells were immediately
processed for 4SC622 immunostaining with PE-AG184 and flow
cytometry analysis. Ninety-three percent of the cells stained
positive for cell surface 4SC622. Alternatively, 1 .mu.g/ml 4SC622
was added to RGC1 cells for 1 hour, then the cells were washed and
incubated in culture medium without 4SC622 with PE-AG184 for 18
hours. Flow cytometry analysis following immunostaining for 4SC622
showed that 9% of the cells retained 4SC622 on the cell surface. To
further characterize the loss of surface-bound 4SC622, purified
4SC622 protein was added to the media of RGC1 and parental CHO K1
cells, then levels of 4SC622 in the media were measured over time.
4SC622, added to 2 .mu.g/ml to the culture media in a 10 cm plate,
was significantly lower in RGC1 conditioned medium after 3 days
incubation as compared to the CHO K1 control. These results show
that the concentration of 4SC622 in the culture medium is reduced
by the presence of hFc.gamma.RI on the cell surface. The results
suggest that the depletion of 4SC622 from the media was the result
of hFc.gamma.RI-4SC622 complex internalization. This
internalization of receptor-ligand complexes may facilitate the
effective removal of all 4SC622 from non-expressing cells in the
presence of blocking IgG during the 18-hour blocking step.
Example 5: Construction of CHO K1 Cell Lines with Inducible
hFc.gamma.RI Expression
[0121] Flow cytometry-based autologous secretion trap (FASTR.TM.)
methods that utilize the hFc.gamma.RI allow rapid isolation of high
expression clones. However, if hFc.gamma.RI mediates turnover of
Fc-tagged proteins, then the realized production of the secreted
protein by engineered hFc.gamma.RI expressing cells would be higher
if hFc.gamma.RI expression could be inhibited during the production
period. To this end, a CHO K1 cell line in which the expression of
hFc.gamma.RI is induced by tetracycline, or the analog doxycycline,
was constructed. In this system, CHO K1 cells were first engineered
to express the tetracycline repressor protein (TetR) and
hFc.gamma.RI was placed under transcriptional control of a promoter
whose activity was regulated by TetR. Two tandem TetR operators
(TetO) were placed immediately downstream of the CMV-MIE
promoter/enhancer in pTE084 to generate pTE158. Transcription of
hFc.gamma.RI from the CMV-MIE promoter in pTE158 was blocked by
TetR in the absence of tetracycline or some other suitable inducer.
In the presence of inducer, TetR protein was incapable of binding
TetO and transcription of hFc.gamma.RI occurred.
[0122] CHO K1 cells were transfected with pcDNA6/TR, a plasmid that
confers resistance to blasticidin in which expression of TetR
originates from the CMV-MIE promoter (Invitrogen; Carlsbad,
Calif.). After two weeks of selection with 2.5 .mu.g/ml blasticidin
(invitrogen), the stable transfectants were pooled. This pool was
then transfected with pTE158, a plasmid that confers resistance to
G418 in which the expression of hFc.gamma.RI is dependent on a
CMV-MIE/TetO hybrid promoter. The cells consecutively transfected
with pcDNA6/TR and pTE158 were selected with 400 .mu.g/mIG418 and
2.5 .mu.g/ml blasticidin for 12 days then pooled. The pool was
induced for two days by the addition of 1 .mu.g/ml doxycycline then
stained with FITC-hFc to identify cells that express hFc.gamma.RI.
The top 5% of cells expressing hFc.gamma.RI were collected as a
pool, expanded for 6 days in the absence of doxycycline, and were
again stained with FITC-hFc for the presence of hFc.gamma.RI. Cells
that did not stain for hFc.gamma.RI were collected and expanded in
culture medium containing 1 .mu.g/ml of doxycycline for three days.
The pool was then stained for the presence of hFc.gamma.RI and were
isolated by flow cytometry. Cells that expressed the highest levels
of hFc.gamma.RI (top 1%) were sorted onto 96 well plates at one
cell per well. These cells presumably contained cell that had low
non-induced expression levels of Fc.gamma.R1 and high inducible
levels of Fc.gamma.R1. After expansion, the induction of
hFc.gamma.RI by doxycycline in 20 clones was confirmed by
immunostaining with FITC-hFc and flow cytometry. One clone was
chosen for further characterization and was named RGC10.
[0123] In the absence of doxycycline, RGC10 did not express
detectable levels of hFc.gamma.RI, whereas high levels of
hFc.gamma.RI were observed in cells that were induced with 1
.mu.g/ml of doxycycline for three days. The mean fluorescence of
RGC10 cells increased by more than 1,000 fold after induction by
doxycycline.
Example 6: Isolation of 4SC622-Producing Cell Lines from RGC10
[0124] RGC10 cells were transfected with pEE14.1-622, and
MSX-resistant cells were pooled after selection with 25 mM MSX for
two weeks. Expression of hFc.gamma.RI was induced by the addition
of 1 .mu.g/ml of doxycycline to the culture medium for three days.
One mg/ml rat IgG was added to the culture medium containing
doxycycline 18 hours prior to staining with polyclonal
FITC-conjugated anti-human IgG (H+L) F(ab')2 fragment and analysis
by flow cytometry. Cells that expressed the highest levels of
4SC622 (top 1%) were sorted into 96 well plates at 1 cell per well.
Without induction of hFc.gamma.RI expression by doxycycline,
staining with polyclonal FITC-conjugated anti-human IgG (H+L)
F(ab').sub.2 fragment fails to detect cell surface bound 4SC622.
Sixty clones were expanded in the absence of doxycycline. The
specific productivity of the 13 highest producers was determined by
Pandex assay. The specific productivity of clone 1C2 was 17.8
pg/cell/day, significantly better than the 12 pg/cell/day observed
for the best 4SC622 cell line previously isolated using the
unregulated hFc.gamma.RI cell line RGC1.
Example 7: Sp2/0 Myeloma Cells can be Engineered to Express a Cell
Surface Capture Protein
[0125] In this example, the Sp2/0-Ag14 myeloma cell line was
engineered to stably express hFc.gamma.RI to demonstrate that the
autologous secretion trap method was applicable to cell lines other
than CHO. The gene for hFc.gamma.RI was introduced into the myeloma
cell by retroviral infection. The plasmid pLXRN (Clontech; Palo
Alto, Calif.), a retroviral DNA vector wherein a gene of interest
may be expressed from the upstream Moloney murine sarcoma virus
long terminal repeat (MoMuSV LTR) promoter, was used to generate
retrovirus encoding the hFc.gamma.RI gene. The 1,363 bp Xho I
fragment from pTE084, encoding the human Fc.gamma.RI gene, was
cloned into the Xho I site of pLXRN. A plasmid in which
hFc.gamma.RI cDNA expression was dependent on the MoMuSV LTR was
chosen and named pTE255.
[0126] Pantropic retrovirus for the expression of hFc.gamma.RI was
generated essentially following the manufacturer's guidelines. The
packaging cell line GP-293, a HEK 293-based cell line that stably
expresses the viral gag and pol proteins (Clontech; Palo Alto,
Calif.), was co-transfected with 10 mg each of pVSV-G and pTE255.
The plasmid pVSV-G allows expression of the viral envelope protein
VSV-G that confers broad host range upon the infective
particles.
[0127] Construction of Sp2-hFc.gamma.RI-4.
[0128] The pantropic hFc.gamma.RI retrovirus was used to infect
1.times.10.sup.7 Sp2/0-Ag14 myeloma cells (American Type Culture
Collection; Manassas, Va.) at a multiplicity of about 10 infective
particles per cell. Three days after infection, cells were stained
for 1 hour then washed twice with PBS prior to analysis by flow
cytometry. Those cells expressing hFc.gamma.RI, as indicated by
bound FITC-hFc, were collected as a pool by flow cytometry. The
pool was expanded for 13 days then again stained with FITC-hFc and
cells expressing hFc.gamma.RI were collected as a pool by flow
cytometry. These sorted cells were cultured in 10% fetal bovine
serum 90% Dulbecco's Modified Eagle's Medium (DMEM) with 4.5 g/I
glucose and 4 mM glutamine for 3 weeks, stained with FITC-hFc, and
the cells with mean fluorescence in the top 1% of the population
were cloned by single cell sorting. After expansion, 24 clones were
examined by flow cytometry for expression of hFc.gamma.RI, as
described above, and one clone, Sp2-hFc.gamma.RI-4, was chosen for
additional characterization.
[0129] Isolation of Sp2-hFc.gamma.RI-4 Cells Expressing 4SC622
Protein.
[0130] Sp2-hFc.gamma.RI-4 cells (1.times.10.sup.7) were transfected
with pTE209, a plasmid that allows constitutive expression of
4SC622 from the CMV-MIE promoter and confers resistance to
hygromycin. The transfected cells were placed in medium containing
10% FCS, 90% D-MEM and 400 .mu.g/ml hygromycin for 14 days.
Hygromycin-resistant cells were incubated with 1 mg/ml rabbit IgG
for eighteen hours prior to staining with polyclonal
FITC-conjugated anti-human IgG (H+L) F(ab').sub.2 fragment. Cells
were stained for 1 hour then washed twice with PBS prior to
analysis by flow cytometry. Labeled cells were collected as a pool
by flow cytometry then cultured for 5 days and sorted as described
above. Cells from the expanded pool that bound the most polyclonal
FITC-conjugated anti-human IgG (H+L) F(ab').sub.2 fragment, top 1%
population, were then cloned by single cell sorting. Production of
4SC622 from ten clones was analyzed by ELISA and all 10 clones were
found to express 4SC622; clone 5H11 produced 4SC622 at 0.5 pg per
cell per day. These data showed that clones secreting 4SC622 were
efficiently isolated by the autologous secretion trap method from a
heterogeneous pool of cells derived from stable transfection of
Sp2-hFc.gamma.RI-4 cells with pTE209.
[0131] To confirm that 4SC622 was autologously displayed on the
surface of myeloma cells expressing both 4SC622 and hFc.gamma.RI,
clone 5H11 was incubated with 1 mg/ml rabbit IgG for 18 hours then
stained with FITC-conjugated anti-human IgG (H+L) F(ab').sub.2
fragment and found to display cell surface 4SC622. Secreted protein
was displayed under conditions in which cross-feeding was blocked
by rabbit IgG, demonstrating the autologous display of 4SC622.
These data indicated that the autologous secretion trap method
described above was not limited to CHO cells and may be extended to
myeloma and other cell types as well.
Example 8. Protein G Chimeric Protein can Function as a Cell
Surface Capture Protein
[0132] To demonstrate the application of the autologous secretion
trap method to a cell surface capture protein other than
hFc.gamma.RI, a cell line expressing Protein G was constructed.
Protein G, from the Streptococcus strain G148, binds to all human
and mouse IgG subclasses, and as such has utility for the isolation
of recombinant cells expressing antibodies or IgG Fc fusion
proteins. To demonstrate that the Protein G IgG Fc binding domain
could be used as a cell surface capture protein capable of binding
to all human and mouse IgG subclasses, we constructed a CHO line
expressing a chimeric protein comprised of the Fc binding domain of
Protein G fused to the hFc.gamma.RI transmembrane and intracellular
domain. The Fc binding domain of Protein G contains three
homologous repeats of 55 amino acids long (Guss et al., (1986) EMBO
5:1567 and Sjobring et al., (1991) J. Biol. Chem. 266:399) and each
repeat is capable of binding one IgG Fc. To improve the expression
of this chimeric protein in CHO cells, we constructed a synthetic
DNA in which the signal sequence from the mouse ROR1 gene was fused
to the Fc binding domain, amino acids 303 to 497 of Protein G
(accession # X06173) (SEQ ID NO:1). This synthetic DNA was
generated by a combination of oligonucleotide annealing, gap
filling, and PCR amplification. The synthetic DNA was then fused,
by PCR, to DNA encoding the transmembrane and intracellular
domains, amino acids 279 to 374 (SEQ ID NO:2), of hFc.gamma.RI
(accession M21091). The resultant DNA encoding the Protein
G/hFc.gamma.RI chimeric protein was cloned into pTE158 downstream
of the CMV-MIE promoter, replacing the gene encoding hFc.gamma.RI,
to yield the plasmid pTE300.
[0133] A CHO K1 cell line adapted to grow in serum-free medium,
RGC14, was transfected with pTE300, and after three days 400
.mu.g/ml G418 was added to the culture medium to select for stable
integration of pTE300. Two weeks after the start of selection, the
cells were stained with FITC-hFc to identify cells that expressed
hFc.gamma.RI. These cells were analyzed by flow cytometry and cells
expressing hFc.gamma.RI were collected as a pool. The cells were
expanded for 10 days and the population of cells expressing
hFc.gamma.RI was again isolated by flow cytometry. The cells were
again expanded, stained with FITC-hFc, and single cells expressing
high levels of the Protein G/hFc.gamma.RI chimeric protein were
isolated by flow cytometry. Single cells that stained positive for
FITC-hFc binding were sorted into medium composed of 10% fetal
bovine serum, 90% Ham's F12, and 400 .mu.g/ml G418. After two weeks
incubation, 48 clones were examined for binding to bovine IgG
present in the culture medium by staining with FITC-conjugated
anti-bovine IgG F(ab')2 fragment (Jackson ImmunoResearch
Laboratories, West Grove, Pa.). One clone, RGC18 that stained
positive with this antibody was chosen for further
characterization.
[0134] Isolation of expression clones in RGC18: RGC18 cells
(6.times.10.sup.6) were transfected with pTE209 and selected for
integration of the plasmid by growth in 400 .mu.g/ml hygromycin for
18 days. Hygromycin-resistant cells were incubated with 1 mg/ml
rabbit IgG for eighteen hours prior to staining with polyclonal
FITC-conjugated anti-human IgG (H+L) F(ab').sub.2 fragment. Cells
were stained for 1 hour then washed twice with PBS prior to
analysis by flow cytometry. The most fluorescent cells (top 5%)
were isolated by single cell sorting and expanded for 3 weeks. Ten
clones were examined for 4SC622 secretion. All clones tested
secreted 4SC622 at high level, and the best clone, RGC19, had a
specific productivity of 6.4 pg/cell day. This result demonstrated
that 4SC622-expressing cells were efficiently isolated from a
heterogeneous pool of cells derived from stable transfection of
RGC18 with pTE209 by the autologous secretion trap method.
Furthermore, these data clearly demonstrated that a fragment of
Protein G could be engineered to include a signal sequence and
transmembrane domain, and function as a cell surface capture
protein.
[0135] To confirm that 4SC622 was autologously displayed on the
surface of RGC19 cells expressing both Protein G/hFc.gamma.RI
chimeric protein and 4SC622, RGC19 was incubated with 1 mg/ml
rabbit IgG for 18 hours then stained with FITC-conjugated
anti-human IgG (H+L) F(ab).sub.2 fragment and analyzed by flow
cytometry. RGC19 cells were found to possess cell surface 4SC622
under these conditions in which cross-feeding was blocked by rabbit
IgG, suggesting autologous display of 4SC622. Rabbit IgG
effectively blocked binding of exogenous 4SC622 protein to RGC18
cells, but did not block display of 4SC622 on the cell surface of
cells expressing 4SC622. These data demonstrated that the
properties of the Protein G/hFc.gamma.RI chimeric protein were
similar to those of hFc.gamma.RI as a cell surface capture protein,
and suggested that the autologous secretion trap method can employ
other proteins as cell surface capture proteins.
Example 9: Isolation of Antibody-Producing Cells from RGC10
[0136] To demonstrate the utility of the autologous secretion trap
method for the isolation of CHO cell lines that express recombinant
antibodies we cloned the DNA encoding variable light and variable
heavy genes from the KD5 hybridoma. KD5 is a hybridoma that
expresses a monoclonal antibody specific for the human Tie-2
receptor.
[0137] The mouse IgG constant region gene sequences were cloned
from 500 ng of mouse spleen polyA+ RNA (Clontech, Palo Alto,
Calif.). Single stranded cDNA was synthesized using SuperScript
First-Strand Synthesis System for RT-PCR, primed with 50 ng of
random hexamers (Invitrogen Life Technologies, Carlsbad, Calif.).
The mouse kappa light constant DNA sequence (accession # Z37499)
was amplified from this cDNA by PCR using the primers 5' mCLK1
(Z37499) (5'-CGGGCTGATG CTGCACCAAC TGTATCCATC TTC-3') (SEQ ID NO:3)
and 3' mCLK1 (Z37499) (5'-ACACTCTCCC CTGTTGAAGC TCTTGACAAT GGG-3')
(SEQ ID NO:4). The mouse IgG2a constant region DNA sequence
(accession # AJ294738) was also amplified from this cDNA by PCR
using the primers 5' mCH2a (AJ294738) (5'-GCCAAAACAA CAGCCCCATC
GGTCTATCCA C-3') (SEQ ID NO:5) and 3' mCH2a (AJ294738)
(5'-TCATTTACCC GGAGTCCGGG AGAAGCTCTT AGTCG-3') (SEQ ID NO:6). The
PCR products were cloned into pCR2.1-TOPO using TOPO TA Cloning kit
(Invitrogen Life Technologies, Carlsbad, Calif.) and the sequence
of the constant regions were verified.
[0138] The KD5 variable region genes were amplified by RT-PCR from
KD5 hybridoma mRNA and cloned into pCR2.1-TOPO using the heavy and
light chain variable region primer mixes from Amersham-Pharmacia
Biotech (Piscataway, N.J.). The variable heavy chain gene was PCR
amplified using the pCR2.1-TOPO cloned variable region as template
with the primers 5' BspMI/KD5VH N-term (5'-GAGAGTACCT GCGTCATGCA
GATGTGAAAC TGCAGGAGTC TGGCCCT-3') (SEQ ID NO:7) and 3' BspMI/KD5VH
C-term (5'-GAGAGACCTG CGTCAGCTGA GGAGACGGTG ACCGTGGT-3') (SEQ ID
NO:8), digested with BspMI and ligated to the BsaI-digested IgG2a
constant heavy gene PCR fragment amplified with the primers 5'
BsaI/CH2a N-term (5'-GAGAGGGTCT CACAGCCAAA ACAACAGCCC CATCG-3')
(SEQ ID NO:9) and 3' BsaI/CH2a C-term (5'-GAGAGGGTCT CCGGCCGCTC
ATTTACCCGG AGTCCGGG AGAA-3') (SEQ ID NO:10). This fragment was then
ligated into the BspMI and NotI sites of pRG882. The resulting
plasmid, pTE317, was capable of expressing the KD5 recombinant
heavy chain gene, fused to the mROR1 signal sequence, from the
CMV-MIE promoter. The variable light chain gene was PCR amplified
using the pCR2.1-TOPO cloned variable region as template with the
primers 5' BsmBI/KD5VL N-term (5'-GAGAGCGTCT CATGCAGACA TCCAGATGAC
CCAGTCTCCA-3') (SEQ ID NO:11) and 3' BsmBI/KD5VL C-term
(5'-GAGAGCGTCT CACAGCCCGT TTTATTTCCA GCTTGGTCCC-3') (SEQ ID NO:12),
digested with BsmBI and ligated to the BsaI-digested kappa constant
light gene PCR fragment amplified with the primers 5' BsaI/CLK
N-term (5'-GAGAGGGTCT CAGCTGATGC TGCACCAACT GTATCC-3') (SEQ ID
NO:13) and 3' BsaI/CLK C-term (5'-GAGAGGGTCT CAGGCCGCTC AACACTCTCC
CCTGTTGAAG CTCTTGAC-3') (SEQ ID NO:14). This fragment was then
ligated into the BspMI and NotI sites of pRG882. The resulting
plasmid, pTE316, was capable of expressing the KD5 recombinant
light chain gene, fused to the mROR1 signal sequence, from the
CMV-MIE promoter.
[0139] The 1450 bp EcoRI-NotI fragment from pTE317, encoding the
KD5 heavy chain gene, was cloned into the EcoRI and NotI sites of
pRG980, a vector that confers resistance to hygromycin and allows
expression of recombinant genes for the UbC promoter, to yield
plasmid pTE322. Similarly, the 750 bp EcoRI-NotI fragment from
pTE316, encoding the KD5 light chain gene, was cloned into the
EcoRI and NotI sites of pRG985, a vector that confers resistance to
puromycin and allows expression of recombinant genes for the UbC
promoter, to yield plasmid pTE324. RGC10 cells (5.times.10.sup.6)
were transfected with 3 .mu.g pTE322 and 3 .mu.g pTE322 and
selected for integration of the plasmids by growth in F12 medium
supplemented with 10% fetal calf serum with 20 .mu.g puromycin and
400 .mu.g/ml hygromycin for 14 days. Expression of hFc.gamma.RI was
induced by the addition of 1 .mu.g/ml of doxycycline to the culture
medium for three days. Double-resistant cells were incubated with 1
mg/ml rabbit IgG for eighteen hours prior to staining with goat
polyclonal FITC-conjugated anti-mouse IgG (Fc.gamma.) F(ab').sub.2
fragment (Jackson ImmunoResearch Laboratories, West Grove, Pa.).
Cells were stained for 1 hour then washed twice with PBS prior to
analysis by flow cytometry. The most fluorescent cells (top 5%)
were isolated as a pool and expanded for 10 days, after which the
protocol was repeated but the top 1% most fluorescent cells were
isolated as a pool. This pool was expanded for 10 days then the top
0.1% most fluorescent cells were isolated as single cells into
96-well plates. Clones were analyzed by ELISA for expression of
antibody and seven clones were chosen from 53 clones analyzed. The
average specific productivity of these clones was 35 pg/cell/day
and the best clone expressed the recombinant KD5 monoclonal
antibody at 54 pg/cell/day.
Example 10: FASTR.TM. Screens Unaffected by CSCP Expression
Level
[0140] To demonstrate that the expression level of the CSCP does
not significantly affect the ability to isolate cells expressing an
associated sPOI, FASTR.TM. screens for the same sPOI in two
different host cell lines that each express the same CSCP but at
either a high level or a low level were compared.
[0141] The FASTR.TM. host cell line RGC10 was selected for
high-level expression of hFc.gamma.RI protein by stable integration
of pTE158 and was found to contain 40 hFc.gamma.RI integrated gene
copies. A new cell line, RS527, that expressed hFc.gamma.RI protein
at a lower level, was generated from CHO K1 after stable
transfection and selection for single copy gene integration. RS527
cells expressed significantly less hFc.gamma.RI protein than RGC10
cells as determined by Western blot analysis of whole cell lysates
of the FASTR.TM. cell lines.
[0142] Briefly, RGC10 and RS527 cells were transfected with pTE462,
a plasmid capable of expressing a secreted hFc-fusion protein
Rc1-hFc and conferring resistance to hygromycin. The transfected
cultures were selected with hygromycin for two weeks. The
hygromycin-resistant cells were induced with 1 pg/ml doxycycline
(Dox) and blocked with rabbit IgG overnight, following the
FASTR.TM. method described herein. The next day, the RGC10/pTE462
and RS527/pTE462 cultures were stained by a FITC-conjugated
antibody specific for hFc and then analyzed by flow cytometry.
Three cell bins R4, R5, and R6 marking cells with low, medium, and
high fluorescence respectively were sorted from each host line and
expanded in tissue culture.
[0143] To compare Rc1-hFc protein production level from the six
cell bins, six cultures were set up using equal number of cells for
each bin. Three days later, conditioned media were collected. The
Rc1-hFc protein titers in the conditioned media were determined by
ELISA and were plotted against mean fluorescence of the respective
cell bins. For both RGC10 and RS527 host lines, there was a similar
correlation between mean fluorescence (amount of Rc1-hFc displayed
on the cell surface) and sPOI protein production levels of the
isolated cell pools. Most significantly, the sPOI titers in the two
high fluorescence R6 bins derived from RGC10 and RS527 were
similar. These data demonstrate that the expression level of the
CSCP in a FASTR.TM. host cell line does not significantly affect
the use of that host to isolate transfected cells based on
expression level of a sPOI.
Example 11: Tie2 Receptor as a Cell Surface Capture Protein
[0144] Cell surface capture proteins (CSCP's) other than
Fc.gamma.R1 can be used in the methods described herein. In this
example, the Tie2 receptor functions as a CSCP and is used to
isolate cells expressing a Tie-specific ScFv.sub.C1b-Fc fusion
protein made from the C1b monoclonal antibody that specifically
binds the extracellular domain of Tie2 receptor. Although the CSCP
for ScFv.sub.C1b-Fc can be hFcgRI, this example demonstrates that
Tie2 can also be used as the CSCP for ScFv.sub.C1b-Fc.
[0145] To construct an inducible Tie2 CSCP cell line, CHO K1 was
first stably transfected with the TetR plasmid pcDNA6/TR. The
blasticidin-resistant cell pool was then stably transfected with
pTE259, a plasmid that allows inducible expression of a protein
comprised of the extracellular domain and transmembrane domain of
Tie2. Inducible cell clones were isolated by flow cytometry after
staining with an antibody specific for Tie2. The RGC54 clone was
chosen to study the feasibility of FASTR.TM. for the expression of
ScFv.sub.C1b-Fc.
[0146] RGC54 cells were stably transfected with pTE988, a plasmid
capable of expressing the secreted hFc-fusion protein
ScFv.sub.C1b-Fc and conferring resistance to hygromycin. The
transfected culture was selected with hygromycin for two weeks. The
hygromycin-resistant cells were induced with Dox and blocked with 1
mg/ml of purified C1b mAb. The C1b monoclonal antibody was the
source of the variable regions in ScFv.sub.C1b-Fc. The next day,
the cell pool was stained by a FITC-conjugated antibody specific
for hFc and then analyzed by flow cytometry. Three cell bins R6,
R7, and R8 marking cells with high, medium, and low fluorescence
respectively were sorted and expanded in tissue culture. Three
cultures were set up using an equal number of cells for each bin to
determine ScFv.sub.C1b-Fc protein production as determined by
ELISA. A correlation existed between mean fluorescence (amount of
ScFv.sub.C1b-Fc binding to Tie2 on the cell surface) and
ScFv.sub.C1b-Fc protein production levels of the isolated cell
pools.
[0147] These data show that CSCP other than hFc.gamma.RI can serve
as a CSCP, and also suggest that any receptor may be converted into
a CSCP by removal of its cytoplasmic domain. These data also
demonstrate that an antigen can be made into a CSCP and used for
FASTR.TM. screening cells expressing an antigen-specific
antibody-related molecule.
Example 12: Effective FASTR.TM. Screens with CSCP:sPOI Pairs Having
Low Affinity
[0148] Angiopoetin-1 is a ligand for the Tie2 receptor. A chimeric
protein comprising angiopoetin-1 receptor binding domain and hFc
(FD1-hFc) binds to Tie2 with an affinity constant of 174 nM as
determined by BIAcore.TM.. FD1-hFc and Tie2 were chosen as sPOI and
CSCP, respectively, to determine if a minimum affinity between CSCP
and sPOI is required for FASTR.TM. screens.
[0149] In cell decoration experiments, exogenously added FD1-hFc
bound specifically to RGC54 cells through Tie2. To determine if the
affinity between Tie2 and FD1-hFc is sufficient to allow FASTR.TM.
screening, RGC54 cells were stably transfected with pTE942, a
plasmid capable of expressing the secreted hFc-fusion protein
FD1-hFc and conferring resistance to hygromycin. The transfected
culture was selected with hygromycin for two weeks. The
hygromycin-resistant cells were induced with Dox and blocked with 1
mg/ml of purified FD1-mFc comprising mouse IgG1 Fc. The next day,
the cell pool was stained by a FITC-conjugated antibody specific
for hFc and then analyzed by flow cytometry. Three cell bins R6,
R7, and R8 marking cells with high, medium, and low fluorescence,
respectively, were collected. Cultures were set up using equal
number of cells for each bin to determine FD1-hFc protein
production levels in the conditioned media as determined by ELISA.
There was a correlation between mean fluorescence (FD1-Fc binding
to cell surface-bound Tie2) and FD1-hFc protein production levels
of the isolated cell pools. The bin with the highest fluorescence
produced the most FD1-hFc.
[0150] These data demonstrate that a CSCP:sPOI pair with low
affinity (174 nM KD) can be used for effective FASTR.TM. screens.
Importantly, the dissociation t.sub.1/2 for FD1-Fc: Tie2 binding is
less than 2 minutes, suggesting that any CSCP:sPOI pair with a
measurable affinity can work in FASTR.TM. screens. In addition,
this experiment also shows that a non-Fc.gamma.RI receptor may be
used as the CSCP to isolate cells expressing its ligand.
Example 12: Fusing a Transmembrane Domain onto an ScFv Makes a
Functional CSCP
[0151] An CSCP can be any cell surface-bound protein that has a
measurable affinity to the sPOI. To demonstrate this, a totally
synthetic CSCP was constructed by fusing the transmembrane domain
from the PDGF receptor to an ScFv containing the variable regions
from the murine kappa chain-specific monoclonal antibody HB58. A
FASTR.TM. host was constructed that expresses this chimeric protein
(ScFv.sub.HB58-TM.sub.PDGFR) and was used to isolate cells
expressing the angiopoeitin-2 FD domain-specific P12 antibody.
[0152] The RS655 cell line, derived from CHO K1, constitutively
expresses ScFv.sub.HB58-TM.sub.PDGFR. Cells expressing
ScFv.sub.HB58-TM.sub.PDGFR can be stained by sequential incubation
with P12 mAb, FD2-hFc, and FITC-conjugated anti-hIgG-P12 captured
on the cell surface by the HB58 ScFv was detected by its affinity
for FD2, which in turn was detected by recognition of the hFc tag.
RS656 cells were derived from RS655 cells after stable transfection
with a plasmid encoding the gene for eYFP. Nearly 100% of RS656
cells were eYFP-positive, and most (76%) maintained expression of
ScFv.sub.HB58-TM.sub.PDGFR as detected by binding to FD2-hFc.
[0153] RS655 cells were stably transfected with pTE693, a plasmid
capable of expressing the heavy and light chains of the P12
antibody, and conferring resistance to puromycin. The transfected
culture was selected with puromycin for two weeks to yield a pool
of cells that were heterogeneous with regard to P12 mAb expression
(RS655/pTE693).
[0154] To determine if ScFv.sub.HB58-TM.sub.PDGFR could function as
a CSCP and facilitate isolation of antibody-producing cells from
non-producers, equal numbers of RS656 cells and RS655/pTE693 cells
were mixed and co-cultured. When P12 expressed from RS655/pTE693
cells was allowed to diffuse and bind to ScFv.sub.HB58 on the
surface of RS656 cells a large population of yellow cells were also
positive for binding FD2-hFc. However, if the ScFv.sub.HB58 on the
surface of RS656 was bound with excess murine IgG, then only
non-yellow cells were positive for binding FD2-hFc, demonstrating
that expressing cells were effectively separated from
non-expressing cells.
[0155] These data demonstrate that an ScFv can be made into a
functional CSCP by targeting it to the cell membrane. The data also
show that FASTR.TM. allows cells expressing a secreted antibody to
be detected with the antibody's antigen.
Example 13: A Protein of Interest Comprising a T Cell Receptor
Variable Region
[0156] A flow cytometry-based autologous secretion trap (FASTR.TM.)
method for isolating high expression clones of a cell line that
expresses a protein of interest that is a TCR-Fc is prepared in a
manner analogous to preparing a cell line that expresses an
antibody of interest. High expression clones are identified by
screening cells that display on their surface the TCR-Fc of
interest bound to hFc.gamma.R.
[0157] In these examples, the CHO K1 cell line RGC10, comprising an
inducible Fc.gamma.R1 as a cell surface capture molecule, is
employed. RGC10 is made to express recombinant TCR-Fc's by cloning
TCR variable regions, in frame, to a human Fc region either
directly in frame or with a linker sequence between the TCR
variable regions and the human Fc region.
[0158] To make a protein of interest that is a dimer comprising an
Fc-linked TCR .alpha. variable domain and an Fc-linked TCR .beta.
variable domain, RGC10 is transfected with two vectors: a first
vector capable of expressing a TCR .alpha. variable domain fusion
protein with a human Fc sequence, and a second vector capable of
expressing a TCR .beta. domain fusion protein with the same human
Fc sequence. Each vector includes leader sequence (e.g., a
secretion signal sequence) 5' with respect to the TCR variable
region, and a selectable marker that is a drug resistance gene.
Following each vector transfection, cells containing the vector are
selected by an appropriate drug selection. The selection results in
an RGC10 cell line having both the first and the second vectors.
Cells expressing proteins of interest can be detected by one or
more of an antibody to the .beta. variable domain, an antibody to
the .alpha. variable domain, and an antibody to the Fc domain.
[0159] To make a protein of interest that is a dimer comprising
both an .alpha. and a .beta. TCR variable domain fused to an Fc,
RGC10 is transfected with a single vector encoding a protein of
interest that is constructed as follows: a leader sequence (e.g., a
secretion signal sequence), followed by a TCR variable .beta.
domain fused to a linker, where the linker is, in turn, fused to a
TCR variable .alpha. domain, which in turn is fused to an Fc
sequence. Alternatively, the single vector can be constructed as
follows: a leader sequence (e.g., a secretion signal sequence),
followed by a TCR variable .alpha. domain fused to a linker, where
the linker is, in turn, fused to a TCR variable .beta. domain,
which in turn is fused to an Fc sequence. Cells expressing proteins
of interest can be detected by one or more of an antibody to the 6
variable domain, an antibody to the .alpha. variable domain, and an
antibody to the Fc domain.
[0160] To make proteins of interest, as above, which also comprise
a TCR .alpha. and/or TCR .beta. constant domain, the TCR variable
domain (.alpha. or .beta.) is fused to a TCR constant domain (e.g.,
TCR variable domain .alpha. is fused to TCR constant domain
.alpha., and TCR variable domain .beta. is fused to TCR constant
domain .beta.), and the TCR variable+constant domain is fused
directly or through a linker to the Fc domain. Cells expressing
proteins of interest can be detected by one or more of an antibody
to the .beta. variable domain, an antibody to the .alpha. variable
domain, and an antibody to the Fc domain.
[0161] Cells expressing desired amounts of the TCR-Fc are isolated
using the same procedure as used in isolating 4SC622-producing cell
lines described herein, using one or more of an antibody to the
.alpha. variable domain, an antibody to the .beta. variable domain,
an antibody to the .alpha. constant domain, and antibody to the
.beta. constant domain, and an antibody to the Fc domain. Cells
expressing the highest levels of the TCR-Fc are selected as
TCR-Fc-producing cell lines.
Example 14: ScFv-Based CSCP for the Isolation of Multiple IgG
Isotypes and Bispecific Antibodies
[0162] Genetically modified mice, whose immunoglobulin heavy chain
VDJ region and immunoglobulin kappa chain VJ region of their
genomes were replaced with the human orthologs (i.e.,
Velocimmune.RTM. mice; see U.S. Pat. No. 7,105,348, which is herein
incorporated by reference in its entirety), were immunized with
either an Fc fragment of a human IgG4 protein (hFc, or simply Fc;
SEQ ID NO: 26), or a human .DELTA.AdpFc polypeptide containing the
dipeptide mutation (H95R, Y96F by IMGT; also known as Fc*; SEQ ID
NO: 42). Monoclonal antibodies were obtained from the mice and
screened for their ability to bind Fc, Fc*, or antibodies
comprising Fc and/or Fc*. Three antibodies that were capable of
binding Fc (Ab1, Ab2, Ab3) and three that were capable of binding
Fc* (Ab4, Ab5, Ab6) were tested for their ability to bind molecules
having one of the following formats: Fc/Fc, Fc/Fc* (which can be a
bispecific antibody), and Fc*/Fc*.
[0163] Measurements to determine binding affinities and kinetic
constants were made on a Biacore 2000 instrument. Antibodies (each
of Ab1-Ab8) were captured onto an anti-mouse-Fc sensor surface (Mab
capture format), and human Fc (SEQ ID NO 26) homodimers, human Fc*
homodimers (SEQ ID NO:42), or Fc/Fc* heterodimers were injected
over the surface. Kinetic association (k.sub.a) and dissociation
(k.sub.d) rate constants were determined by processing and fitting
the data to a 1:1 binding model using Scrubber 2.0 curve fitting
software. Binding dissociation equilibrium constants (K.sub.D) and
dissociative half-lives (t.sub.1/2) were calculated from the
kinetic rate constants as: K.sub.D (M)=k.sub.d/k.sub.a; and tin
(min)=(ln 2/(60*k.sub.d). As shown in Table 2 antibodies were of 3
distinct categories: Fc specific, Fc* specific, and those showing
no discrimination between Fc and Fc* (non-specific). The Fc
specific antibodies were dependent on amino acids His 95 and/or Tyr
96, since these antibodies do not bind human Fc* with its dipeptide
mutation (H95R, Y96F). In contrast the Fc* specific antibodies were
dependent on Arg 95 and/or Phe 96, since these antibodies do not
bind wild type human Fc.
Example 15: Cell Lines Producing Ab2 and Ab2-Derived
ScFv-Fc.gamma.R Fusion Protein
[0164] The heavy chain and the light chain of the Fc-specific Ab2
were sequenced. To manufacture the recombinant Ab2 antibody, an
expression vector plasmid was constructed that encodes the heavy
chain and an expression vector plasmid was constructed that encodes
the light chain. Both vectors enable expression and secretion of
the respective subunits in a CHO cell. To express the antibody,
both plasmids were transfected into a CHO-K1 cell and stable
transformants were isolated. Expression of the antibody chains was
driven by the constitutive CMV promoter.
TABLE-US-00002 TABLE 2 Affinity of Antibodies - Surface Plasmon
Resonance Studies Anti- POI- t 1/2 Speci- body Target ka
(M.sup.-1s.sup.-1) kd (s.sup.-1) KD (M) (min) ficity Ab1 Fc/Fc
1.07E+05 3.79E-04 3.54E-09 30 Fc Fc/Fc* 8.16E+04 3.01E-04 3.69E-09
38 Fc*/Fc* NB NB NB NB Ab2 Fc/Fc 7.86E+04 3.50E-05 4.45E-10 330 Fc
Fc/Fc* 5.45E+04 1.00-06 1.84E-11 11550 Fc*/Fc* NB NB NB NB Ab3
Fc/Fc 1.77E+05 4.08E-02 2.30E-07 0.3 Fc Fc/Fc* 4.51E+04 2.60E-02
5.77E-07 0.4 Fc*/Fc* NB NB NB NB Ab4 Fc/Fc NB NB NB NB Fc* Fc/Fc*
6.00E+03 1.00E-06 2.00E-10 11550 Fc*/Fc* 2.22E+04 9.56E-06 4.50E-10
1209 Ab5 Fc/Fc NB NB NB NB Fc* Fc/Fc* 3.11E+05 1.00E-06 3.21E-12
11550 Fc*/Fc* 5.57E+05 1.00E-06 1.79E-12 11550 Ab6 Fc/Fc NB NB NB
NB Fc* Fc/Fc* 4.48E+05 7.43E-04 1.66E-09 16 Fc*/Fc* 8.73E+05
5.93E-04 6.79E-10 19 Ab7 Fc/Fc 6.02E+05 2.42E-04 4.02E-10 48 Non-
Fc/Fc* 4.90E+05 2.15E-04 4.39E-10 54 specific Fc*/Fc* 4.46E+05
3.20E-02 7.18E-08 0.4 Ab8 Fc/Fc 2.59E+05 4.88E-04 1.88E-09 24 Non-
Fc/Fc* 1.88E+05 4.02E-04 2.14E-09 29 specific Fc*/Fc* 4.10E+04
3.90E-02 9.60E-07 0.3
[0165] The heavy chain and light chain sequences were used to
develop an anti-Fc ScFv surface capture molecule. To manufacture
the nucleic acid encoding the Ab2-derived anti-Fc ScFv-Fc.gamma.R
surface capture molecule, the Ab2 immunoglobulin heavy chain
variable domain (SEQ ID NO:15) and the Ab2 immunoglobulin light
chain variable domain (SEQ ID NO:16) amino acid sequences were
reverse translated and codon optimized for CHO cell expression.
Likewise, the C-terminal portion of human Fc.gamma.RI was codon
optimized for CHO cell expression. The codon optimized nucleotide
sequences were amplified via polymerase chain reaction and ligated
to form a contiguous nucleic acid sequence (SEQ ID NO:20) that
encodes the ScFv-Fc.gamma.R fusion protein of SEQ ID NO:19.
[0166] The nucleic acid encoding the ScFv-Fc.gamma.R-TM-cyto fusion
protein was inserted into an expression vector using standard PCR
and restriction endonuclease cloning techniques. The resultant
circular plasmid, exemplified in SEQ ID NO:23, comprises a
beta-lactamase-encoding nucleic acid sequence, and two operons. The
first operon comprises a nucleic acid sequence encoding yellow
fluorescence protein (YFP), a variant of green fluorescent protein,
in frame with a neomycin resistance marker, driven by an SV40
promoter (e.g., SEQ ID NO:24). The second operon, which is the
"business-end" of the vector for the purposes of this aspect of the
invention, comprises a nucleic acid sequence encoding the
codon-optimized ScFv-Fc.gamma.R fusion protein, driven by an
hCMV-IE promoter and hCMV intron (e.g., SEQ ID NO:25).
[0167] CHO-K1 cells were transfected with the plasmid of SEQ ID
NO:23. Stable integrants, which have integrated the linear
construct of SEQ ID NO:22 into their genomes, were isolated.
[0168] The circular plasmid contains two Lox sites flanking the
first operon and the second operon, to allow for the integration of
those operons as a linear construct into the genome of the host
cell. The linear construct spanning from the first Lox site to the
second Lox site is exemplified in SEQ ID NO:22 and comprises from
5-prime to 3-prime: SV40 promoter, nucleic acid encoding
neomycin-resistance, IRES, nucleic acid encoding eYFP, SV40
polyadenylation sequence, hCMV-IE promoter, hCMV intron,
Tet-operator sequence (for controlled expression of the
ScFv-Fc.gamma.R-TM-cyto fusion protein), nucleic acid encoding mROR
signal sequence, nucleic acid encoding Ab2 ScFv, nucleic acid
encoding the Fc.gamma.R transmembrane and cytoplasmic portion (SEQ
ID NO: 21), and SV40 polyadenylation sequence.
Example 16: ScFv-Fc.gamma.R-TM-Cyto Surface Capture Targets
[0169] CHO-K1 cells containing the integrated sequence of SEQ ID
NO:22 were transfected with plasmids that encode antibodies of
various subtypes, e.g., IgG1, IgG2, IgG4, an IgG4 bispecific
antibody containing one CH3 domain with the 95R/435R-96F/436F dual
substitution while the other CH3 domain is wild-type (IgG4 Fc/Fc*),
and an IgG1 bispecific antibody of the IgG1 Fc/Fc* format. The
cells were treated with doxycycline to induce production of the
capture molecule along with the antibody. After co-expression of
the antibody and capture molecule, the cells in some cases were
treated with hFc blocking protein, and detection molecule
(FITC-labeled anti-hFab). Table 3 summarizes the results, and
generally shows that the ScFv-Fc.gamma.R surface capture fusion
protein binds IgG4, IgG2, and IgG1 molecules, while the wildtype
Fc.gamma.R surface capture molecule binds IgG1, but not IgG4 or
IgG2.
TABLE-US-00003 TABLE 3 Blocking Molecule Competition Assays
Arbitrary FITC Units (with or without hFc blocking molecule) - Mode
hFc hFc hFc hFc No displace- Antibody No hFc (1 hr) (2 hr) (20 hr)
coat ment? Capture molecule = ScFv-Fc.gamma.R-TM-cyto Detection
molecule = FITC-anti-hFab IgG1 mAb-3 250 120 80 20 10 Yes IgG4
mAb-4 250 100 55 20 10 Yes IgG4 mAb-5 250 70 40 20 10 Yes IgG2
mAb-6 .sup. 200.sup.1 ND ND ND .sup. 12.sup.2 Yes Capture molecule
= hFc.gamma.R Detection molecule = FITC-anti-hFab IgG1 mAb-3 300 80
30 9 3.5 Yes IgG4 mAb-4 100 2 2 2 2 No IgG4 mAb-5 35 5 5 5 5 No
.sup.1+Dox .sup.2-Dox
Example 17: Cell Lines Producing Ab6 and Ab6-Derived
ScFv*-Fc.gamma.R-TM-Cyto
[0170] The heavy chain and the light chain of the Fc-specific Ab6
were sequenced. The amino acid sequence of the light chain was
determined to be SEQ ID NO:41. The amino acid sequence of the heavy
chain was determined to be SEQ ID NO:40. To manufacture the
recombinant Ab6 antibody, an expression vector plasmid was
constructed that encodes the heavy chain and an expression vector
plasmid was constructed that encodes the light chain. To express
the antibody, both plasmids were transfected into a CHO-K1 cell,
stable transformants were isolated, and expression was driven by
the constitutive CMV promoter.
[0171] To manufacture the nucleic acid encoding the Ab6-derived
anti-Fc-specific ScFv*-Fc.gamma.R surface capture molecule, the
immunoglobulin heavy chain variable domain of the Ab6 antibody (SEQ
ID NO:38) and the immunoglobulin light chain variable domain of Ab6
(SEQ ID NO:39) amino acid sequences were reverse translated and
codon optimized for CHO cell expression. Likewise, the C-terminal
portion of human Fc.gamma.RI (SEQ ID NO: 21) was codon optimized
for CHO cell expression. The codon optimized nucleotide sequences
were amplified via polymerase chain reaction and ligated to form a
contiguous nucleic acid sequence (SEQ ID NO:45) that encodes the
anti-Fc* ScFv*-Fc.gamma.R fusion protein (SEQ ID NO:43).
[0172] The nucleic acid encoding the ScFv*-Fc.gamma.R-TM-cyto
fusion protein was inserted into an expression vector using
standard PCR and restriction endonuclease cloning techniques. The
resultant circular plasmid, exemplified in SEQ ID NO:44, comprises
a beta-lactamase-encoding nucleic acid sequence, and two operons.
The first operon comprises a nucleic acid sequence encoding yellow
fluorescence protein (YFP), a variant of green fluorescent protein,
in frame with a neomycin resistance marker, driven by an SV40
promoter (e.g., SEQ ID NO:46). The second operon, which is the
"business-end" of the vector for the purposes of this aspect of the
invention, comprises a nucleic acid sequence encoding the
codon-optimized anti-Fc* ScFv-Fc.gamma.R fusion protein, driven by
an hCMV-IE promoter and hCMV intron (e.g., SEQ ID NO:47).
[0173] CHO-K1 cells were transfected with the plasmid of SEQ ID
NO:44. Stable integrants, which have integrated the linear
construct of SEQ ID NO:48, were isolated.
[0174] The circular plasmid contains two Lox sites flanking the
first operon and the second operon, to allow for the integration of
those operons as a linear construct into the genome of the host
cell. The linear construct spanning from the first Lox site to the
second Lox site is exemplified in SEQ ID NO:48 and comprises from
5-prime to 3-prime: SV40 promoter, nucleic acid encoding
neomycin-resistance, IRES, nucleic acid encoding eYFP, SV40
polyadenylation sequence, hCMV-IE promoter, hCMV intron,
Tet-operator sequence (for controlled expression of the anti-Fc*
ScFv*-Fc.gamma.R fusion protein), nucleic acid encoding mROR signal
sequence, nucleic acid encoding the Ab6-derived anti-Fc*-specific
ScFv*, nucleic acid encoding the Fc.gamma.R transmembrane and
cytoplasmic domain polypeptide (SEQ ID NO: 21), and SV40
polyadenylation sequence.
Example 18: Sorting Bispecific Antibodies
Anti-Fc Capture & Anti-Fc* Detection
[0175] The Ab2-derived anti-Fc-specific ScFv-Fc.gamma.R surface
capture system was tested for its ability to detect and enrich for
cells that produce bispecific antibodies. To assess the ability to
detect bispecific antibodies, which harbor the 95R/435R-96F/436F
substitution in one of the CH3 domains (designated Fc*), various
antibodies were expressed in the Ab2-derived anti-Fc-specific
ScFv-Fc.gamma.R surface capture cell line, using hFc as the
blocking molecule, and a FITC-labeled Ab6 anti-Fc* antibody (e.g.,
mAb with HC of SEQ ID NO:40, and LC of SEQ ID NO:41) as the
detection molecule. The Ab2-derived anti-Fc-specific
ScFv-Fc.gamma.R surface capture cell line was able to detect and
distinguish the bispecific antibody (Fc/Fc*) over any Fc*/Fc* or
Fc/Fc monospecific antibodies using the Fc*-specific Ab6 as the
detection molecule (Table 4). The wildtype Fc.gamma.R surface
capture cell line was not able to distinguish between the Fc/Fe,
Fe/Fe, and Fc/Fc IgG4 species, since Fc.gamma.R is unable to bind,
or binds at very low affinity to IgG4.
Anti-Fe Capture & Anti-Fc Detection
[0176] Conversely, the Ab6-derived anti-Fc-specific
ScFv*-Fc.gamma.R surface capture system was tested for its ability
to detect and enrich for cells that produce bispecific antibodies.
To assess the ability to detect bispecific antibodies, which harbor
the 95R/435R-96F/436F substitution in one of the CH3 domains
(designated Fc*), various antibodies were expressed in the
Ab6-derived anti-Fc-specific ScFv*-Fc.gamma.R surface capture cell
line, using hFc as the blocking molecule, and an Alexa 488-labeled
Ab2 anti-Fc antibody, which recognizes non-substituted CH3, as the
detection molecule. The Ab6-derived anti-Fc-specific
ScFv*-Fc.gamma.R surface capture cell line was able to detect and
distinguish the bispecific antibody (Fc/Fc*) over the Fc*/Fc* or
Fc/Fc monospecific antibodies using the Fc-specific Ab2 as the
detection molecule (Table 4). The Fc.gamma.R surface capture cell
line was not able to distinguish between the Fc/Fe, Fe/Fe, and
Fc/Fc IgG4 species.
TABLE-US-00004 TABLE 4 Detection of Bispecific Antibody - Mean
Fluorescence Intensity (MFI) IgG1 IgG4 Fc/Fc* Fc/ Fc*/ Fc/ Fc/ Fc*/
Fc/ Speci- .sup.1 CSCP .sup.2 DM Fc* Fc* Fc Fc* Fc* Fc ficity
Fc.gamma.R Ab2 500 ND 350 200 200 200 NO Ab6 200 200 200 ND ND ND
NO Anti- 1800 ND 1000 ND ND ND NO hFc ScFv- Ab6 500 15 15 500 15 15
YES Fc.gamma.R Anti- ND ND ND ND ND ND ND hFc ScFv*- Ab2 150 10 10
ND ND ND YES Fc.gamma.R Anti- 200 ND 10 ND ND ND YES hFc .sup.1
Cell surface capture protein .sup.2 Detection molecule
Example 19: Enrichment of Fc/Fc* Bispecific Antibodies
[0177] To assess the ability of the (Ab2-derived) ScFv-Fc.gamma.R
CSCP/(Ab6) anti-Fe DM and the (Ab6-derived) ScFv*-Fc.gamma.R
CSCP/(Ab2) anti-Fc DM systems to sort and enrich bispecific
antibodies, cell lines co-expressing an Fc/Fe IgG4 monoclonal
antibody (IgG4-mAb-2) and the anti-Fc ScFv-Fc.gamma.R fusion
protein, using hFc as the blocking molecule and the FITC-labeled
anti-Fc* (Ab6) antibody as the detection molecule, were subjected
to serial fluorescence activated cell sorting and pooling to enrich
for production of the Fc/Fc* species. Cells yielding Fc/Fc* from
the fifth and sixth series pools were analyzed for total antibody
titer and titers of each antibody format: Fc/Fc*, Fc/Fc, and
Fc*/Fc*. Since the cells encode both a heavy chain encoding the
non-substituted CH3 domain ("Fc", i.e., comprising a histidine at
IMGT position 95 and a tyrosine at IMGT position 96) and a heavy
chain encoding the substituted CH3 domain ("Fe", i.e., comprising
an arginine at IMGT position 95 and a phenylalanine at IMGT
position 96), by purely mathematical Punnett square analysis, the
cell is theoretically expected to produce 25% Fc/Fc, 50% Fc/Fc*,
and 25% Fc*/Fc*. Biologically, however, one might expect
(pre-enrichment) most of the antibody produced to be Fc/Fc.
[0178] As shown in Table 5, cells selected, pooled, and enriched
for bispecific antibody production produced as much as 49% Fc/Fc*
species, with titers of Fc/Fc* bispecific antibodies of at least
about 3.2 g/L.
TABLE-US-00005 TABLE 5 Enrichment of Fc/Fc* bispecific antibody
IgG4-mAb-2 Fc/Fc* Fc/Fc Fc*/Fc* Titer Titer Titer pool Cell line
(g/L) % (g/L) % (g/L) % 5 1 1.2 28 2.2 50 0.99 23 2 1.9 49 1.3 32
0.73 19 3 1.5 47 1.2 40 0.40 13 4 1.6 37 1.3 31 1.3 32 5 1.5 48 1.1
35 0.58 18 6 1.8 47 1.3 33 0.75 20 6 7 2.6 44 2.0 34 1.3 23 8 3.2
42 2.4 31 2.0 27 9 2.1 45 1.5 33 1.0 22 10 2.8 43 2.0 31 1.7 28 11
2.3 44 1.6 31 1.3 24
[0179] Although the foregoing invention has been described in some
detail by way of illustration and example, it will be readily
apparent to those of ordinary skill in the art that certain changes
and modifications may be made to the teachings of the invention
without departing from the spirit or scope of the appended claims.
Sequence CWU 1
1
511195PRTStreptococcus 1Thr Tyr Lys Leu Ile Leu Asn Gly Lys Thr Leu
Lys Gly Glu Thr Thr 1 5 10 15 Thr Glu Ala Val Asp Ala Ala Thr Ala
Glu Lys Val Phe Lys Gln Tyr 20 25 30 Ala Asn Asp Asn Gly Val Asp
Gly Glu Trp Thr Tyr Asp Asp Ala Thr 35 40 45 Lys Thr Phe Thr Val
Thr Glu Lys Pro Glu Val Ile Asp Ala Ser Glu 50 55 60 Leu Thr Pro
Ala Val Thr Thr Tyr Lys Leu Val Ile Asn Gly Lys Thr 65 70 75 80 Leu
Lys Gly Glu Thr Thr Thr Glu Ala Val Asp Ala Ala Thr Ala Glu 85 90
95 Lys Val Phe Lys Gln Tyr Ala Asn Asp Asn Gly Val Asp Gly Glu Trp
100 105 110 Thr Tyr Asp Asp Ala Thr Lys Thr Phe Thr Val Thr Glu Lys
Pro Glu 115 120 125 Val Ile Asp Ala Ser Glu Leu Thr Pro Ala Val Thr
Thr Tyr Lys Leu 130 135 140 Val Ile Asn Gly Lys Thr Leu Lys Gly Glu
Thr Thr Thr Lys Ala Val 145 150 155 160 Asp Ala Glu Thr Ala Glu Lys
Ala Phe Lys Gln Tyr Ala Asn Asp Asn 165 170 175 Gly Val Asp Gly Val
Trp Thr Tyr Asp Asp Ala Thr Lys Thr Phe Thr 180 185 190 Val Thr Glu
195 296PRTHomo sapiens 2Gln Val Leu Gly Leu Gln Leu Pro Thr Pro Val
Trp Phe His Val Leu 1 5 10 15 Phe Tyr Leu Ala Val Gly Ile Met Phe
Leu Val Asn Thr Val Leu Trp 20 25 30 Val Thr Ile Arg Lys Glu Leu
Lys Arg Lys Lys Lys Trp Asp Leu Glu 35 40 45 Ile Ser Leu Asp Ser
Gly His Glu Lys Lys Val Thr Ser Ser Leu Gln 50 55 60 Glu Asp Arg
His Leu Glu Glu Glu Leu Lys Cys Gln Glu Gln Lys Glu 65 70 75 80 Glu
Gln Leu Gln Glu Gly Val His Arg Lys Glu Pro Gln Gly Ala Thr 85 90
95 333DNAartificial sequencesynthetic 3cgggctgatg ctgcaccaac
tgtatccatc ttc 33433DNAartificial sequencesynthetic 4acactctccc
ctgttgaagc tcttgacaat ggg 33531DNAartificial sequencesynthetic
5gccaaaacaa cagccccatc ggtctatcca c 31635DNAartificial
sequencesynthetic 6tcatttaccc ggagtccggg agaagctctt agtcg
35747DNAartificial sequencesynthetic 7gagagtacct gcgtcatgca
gatgtgaaac tgcaggagtc tggccct 47838DNAartificial sequencesynthetic
8gagagacctg cgtcagctga ggagacggtg accgtggt 38935DNAartificial
sequencesynthetic 9gagagggtct cacagccaaa acaacagccc catcg
351042DNAartificial sequencesynthetic 10gagagggtct ccggccgctc
atttacccgg agtccgggag aa 421140DNAartificial sequencesynthetic
11gagagcgtct catgcagaca tccagatgac ccagtctcca 401240DNAartificial
sequencesynthetic 12gagagcgtct cacagcccgt tttatttcca gcttggtccc
401336DNAartificial sequencesynthetic 13gagagggtct cagctgatgc
tgcaccaact gtatcc 361448DNAartificial sequencesynthetic
14gagagggtct caggccgctc aacactctcc cctgttgaag ctcttgac
4815113PRTHomo sapiens 15Gln Leu Gln Gln Ser Gly Ala Glu Leu Ala
Lys Pro Gly Ala Ser Val 1 5 10 15 Lys Met Ser Cys Lys Ala Ser Gly
Tyr Thr Phe Thr Asn Tyr Trp Ile 20 25 30 His Trp Glu Lys Gln Arg
Pro Glu Gln Gly Leu Glu Trp Ile Gly Tyr 35 40 45 Ile Asn Pro Asn
Thr Gly His Thr Glu Tyr Asn Gln Lys Phe Lys Asp 50 55 60 Lys Ala
Thr Leu Thr Ala Asp Arg Ser Ser Ser Thr Ala Tyr Met Gln 65 70 75 80
Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr Phe Cys Ala Arg 85
90 95 Thr Tyr Ser Gly Ser Ser His Phe Asp Tyr Trp Gly Gln Gly Thr
Thr 100 105 110 Leu 16112PRTHomo sapiens 16Ser Asp Ile Val Met Thr
Gln Thr Pro Val Ser Leu Pro Val Ser Leu 1 5 10 15 Gly Asp Gln Ala
Ser Ile Ser Cys Arg Ser Ser Gln Ser Leu Val His 20 25 30 Asn Asn
Gly Asp Thr Phe Leu His Trp Tyr Leu Gln Lys Pro Gly Gln 35 40 45
Ser Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn Arg Phe Ser Gly Val 50
55 60 Pro Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu
Lys 65 70 75 80 Ile Ser Arg Val Glu Ala Glu Asp Leu Gly Val Tyr Phe
Cys Ser Gln 85 90 95 Thr Thr Leu Ile Pro Arg Thr Phe Gly Gly Gly
Thr Lys Leu Glu Ile 100 105 110 1721PRTHomo sapiens 17Val Leu Phe
Tyr Leu Ala Val Gly Ile Met Phe Leu Val Asn Thr Val 1 5 10 15 Leu
Trp Val Thr Ile 20 1861PRTHomo sapiens 18Arg Lys Glu Leu Lys Arg
Lys Lys Lys Trp Asp Leu Glu Ile Ser Leu 1 5 10 15 Asp Ser Gly His
Glu Lys Lys Val Thr Ser Ser Leu Gln Glu Asp Arg 20 25 30 His Leu
Glu Glu Glu Leu Lys Cys Gln Glu Gln Lys Glu Glu Gln Leu 35 40 45
Gln Glu Gly Val His Arg Lys Glu Pro Gln Gly Ala Thr 50 55 60
19334PRTartificial sequencesynthetic 19Gln Val Gln Leu Gln Gln Ser
Gly Ala Glu Leu Ala Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Met Ser
Cys Lys Ala Ser Gly Tyr Thr Phe Thr Asn Tyr 20 25 30 Trp Ile His
Trp Glu Lys Gln Arg Pro Glu Gln Gly Leu Glu Trp Ile 35 40 45 Gly
Tyr Ile Asn Pro Asn Thr Gly His Thr Glu Tyr Asn Gln Lys Phe 50 55
60 Lys Asp Lys Ala Thr Leu Thr Ala Asp Arg Ser Ser Ser Thr Ala Tyr
65 70 75 80 Met Gln Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr
Phe Cys 85 90 95 Ala Arg Thr Tyr Ser Gly Ser Ser His Phe Asp Tyr
Trp Gly Gln Gly 100 105 110 Thr Thr Leu Ile Val Ser Ser Gly Gly Gly
Gly Ser Gly Gly Gly Gly 115 120 125 Ser Gly Gly Gly Gly Ser Asp Ile
Val Met Thr Gln Thr Pro Val Ser 130 135 140 Leu Pro Val Ser Leu Gly
Asp Gln Ala Ser Ile Ser Cys Arg Ser Ser 145 150 155 160 Gln Ser Leu
Val His Asn Asn Gly Asp Thr Phe Leu His Trp Tyr Leu 165 170 175 Gln
Lys Pro Gly Gln Ser Pro Lys Leu Leu Ile Tyr Lys Val Ser Asn 180 185
190 Arg Phe Ser Gly Val Pro Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr
195 200 205 Asp Phe Thr Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Leu
Gly Val 210 215 220 Tyr Phe Cys Ser Gln Thr Thr Leu Ile Pro Arg Thr
Phe Gly Gly Gly 225 230 235 240 Thr Lys Leu Glu Ile Lys Arg Gly Gly
Gly Gly Ser Val Leu Phe Tyr 245 250 255 Leu Ala Val Gly Ile Met Phe
Leu Val Asn Thr Val Leu Trp Val Thr 260 265 270 Ile Arg Lys Glu Leu
Lys Arg Lys Lys Lys Trp Asp Leu Glu Ile Ser 275 280 285 Leu Asp Ser
Gly His Glu Lys Lys Val Thr Ser Ser Leu Gln Glu Asp 290 295 300 Arg
His Leu Glu Glu Glu Leu Lys Cys Gln Glu Gln Lys Glu Glu Gln 305 310
315 320 Leu Gln Glu Gly Val His Arg Lys Glu Pro Gln Gly Ala Thr 325
330 201005DNAartificial sequencesynthetic 20caagtacaac tgcaacaaag
cggagctgaa ctggccaaac caggcgcttc cgtgaagatg 60tcttgtaaag ccagcgggta
tacatttact aattactgga ttcactggga gaagcaaaga 120cctgaacagg
gattggaatg gattggatac attaatccta acaccggaca cacagagtat
180aatcaaaaat tcaaggataa ggccaccctc acagccgaca gatcttcttc
aaccgcctat 240atgcaacttt cttccctcac ttctgaagac tccgcagttt
acttttgcgc acgaacttat 300tctggaagct cccatttcga ctactggggt
caaggaacaa cactgatcgt gtctagcggc 360ggcggagggt ccggcggggg
cggtagcggt ggcggaggtt ctgatattgt catgactcaa 420acacctgtct
ctctgcctgt ttcacttgga gatcaagcta gcatttcctg ccgctctagt
480caatctctcg tccacaacaa cggcgatact ttcttgcatt ggtatctgca
gaaaccaggt 540cagtcaccta aactgcttat atacaaagtc tctaatagat
tctcaggggt gccagatcga 600ttcagtggtt ctgggtccgg tacagatttt
acactcaaga tatccagagt agaagcagaa 660gatctgggcg tgtatttctg
cagtcaaaca acacttattc ctcgtacttt tggaggcggt 720acaaaactgg
agatcaagcg tggaggcgga gggagtgttt tgttttatct ggccgttggg
780ataatgtttc tcgtaaatac agtactttgg gtaacaataa ggaaggaact
gaagagaaag 840aaaaaatggg atctggaaat atcattggac agtggacacg
aaaaaaaagt cacatcatca 900ttgcaagaag accggcactt ggaggaggaa
ctgaaatgtc aagagcaaaa agaagaacaa 960ctgcaagaag gcgtacatag
aaaagaacca cagggagcaa catag 10052182PRTHomo sapiens 21Val Leu Phe
Tyr Leu Ala Val Gly Ile Met Phe Leu Val Asn Thr Val 1 5 10 15 Leu
Trp Val Thr Ile Arg Lys Glu Leu Lys Arg Lys Lys Lys Trp Asp 20 25
30 Leu Glu Ile Ser Leu Asp Ser Gly His Glu Lys Lys Val Thr Ser Ser
35 40 45 Leu Gln Glu Asp Arg His Leu Glu Glu Glu Leu Lys Cys Gln
Glu Gln 50 55 60 Lys Glu Glu Gln Leu Gln Glu Gly Val His Arg Lys
Glu Pro Gln Gly 65 70 75 80 Ala Thr 225759DNAartificial
sequencesynthetic 22acaacttcgt atagcataca ttatacgaag ttatggtacc
aagcctaggc ctccaaaaaa 60gcctcctcac tacttctgga atagctcaga ggcagaggcg
gcctcggcct ctgcataaat 120aaaaaaaatt agtcagccat ggggcggaga
atgggcggaa ctgggcggag ttaggggcgg 180gatgggcgga gttaggggcg
ggactatggt tgctgactaa ttgagatgca tgctttgcat 240acttctgcct
gctggggagc ctggggactt tccacacctg gttgctgact aattgagatg
300catgctttgc atacttctgc ctgctgggga gcctggggac tttccacacc
ggatccacca 360tgggttcagc tattgagcag gatgggttgc atgctggtag
tcccgccgca tgggtcgaac 420gactgtttgg atacgattgg gcccaacaga
ctataggctg ttccgacgct gctgtctttc 480gtctttctgc acaaggtcgt
ccagttctgt tcgtgaaaac cgacttgtcc ggagccctca 540atgagttgca
agacgaagct gcacgactga gttggcttgc caccactggt gtcccatgtg
600ccgcagtact tgacgtcgtc acagaggctg gtcgcgattg gttgctcctt
ggagaagtgc 660ccggccaaga tcttctcagt tcccaccttg cccctgccga
aaaagtttca ataatggctg 720acgctatgag aaggctgcac acccttgacc
ctgccacatg tccattcgat caccaagcca 780aacaccgaat tgaacgagct
agaacccgca tggaagccgg cctcgttgat caagacgatt 840tggatgagga
acaccagggt ctcgcacccg ctgaactctt cgctcgcctc aaagcacgaa
900tgccagacgg agatgacttg gtcgtaaccc acggagatgc ctgccttcct
aacataatgg 960tagagaatgg aagatttagc ggcttcattg attgtggacg
acttggagtt gcagatcggt 1020accaagatat cgctctcgct accagagata
ttgctgaaga attgggcgga gaatgggctg 1080atcggtttct cgtactctac
ggaattgccg cacctgattc ccaacgcatt gctttttacc 1140gtcttctgga
tgagttcttc taaacgcgtc ccccctctcc ctcccccccc cctaacgtta
1200ctggccgaag ccgcttggaa taaggccggt gtgcgtttgt ctatatgtta
ttttccacca 1260tattgccgtc ttttggcaat gtgagggccc ggaaacctgg
ccctgtcttc ttgacgagca 1320ttcctagggg tctttcccct ctcgccaaag
gaatgcaagg tctgttgaat gtcgtgaagg 1380aagcagttcc tctggaagct
tcttgaagac aaacaacgtc tgtagcgacc ctttgcaggc 1440agcggaaccc
cccacctggc gacaggtgcc tctgcggcca aaagccacgt gtataagata
1500cacctgcaaa ggcggcacaa ccccagtgcc acgttgtgag ttggatagtt
gtggaaagag 1560tcaaatggct ctcctcaagc gtattcaaca aggggctgaa
ggatgcccag aaggtacccc 1620attgtatggg atctgatctg gggcctcggt
gcacatgctt tacatgtgtt tagtcgaggt 1680taaaaaacgt ctaggccccc
cgaaccacgg ggacgtggtt ttcctttgaa aaacacgatt 1740gctcgaatca
ccatggtgag caagggcgag gagctgttca ccggggtggt gcccatcctg
1800gtcgagctgg acggcgacgt aaacggccac aagttcagcg tgtccggcga
gggcgagggc 1860gatgccacct acggcaagct gaccctgaag ttcatctgca
ccaccggcaa gctgcccgtg 1920ccctggccca ccctcgtgac caccttcggc
tacggcctgc agtgcttcgc ccgctacccc 1980gaccacatga agcagcacga
cttcttcaag tccgccatgc ccgaaggcta cgtccaggag 2040cgcaccatct
tcttcaagga cgacggcaac tacaagaccc gcgccgaggt gaagttcgag
2100ggcgacaccc tggtgaaccg catcgagctg aagggcatcg acttcaagga
ggacggcaac 2160atcctggggc acaagctgga gtacaactac aacagccaca
acgtctatat catggccgac 2220aagcagaaga acggcatcaa ggtgaacttc
aagatccgcc acaacatcga ggacggcagc 2280gtgcagctcg ccgaccacta
ccagcagaac acccccatcg gcgacggccc cgtgctgctg 2340cccgacaacc
actacctgag ctaccagtcc gccctgagca aagaccccaa cgagaagcgc
2400gatcacatgg tcctgctgga gttcgtgacc gccgccggga tcactctcgg
catggacgag 2460ctgtacaagt aatcggccgc taatcagcca taccacattt
gtagaggttt tacttgcttt 2520aaaaaacctc ccacacctcc ccctgaacct
gaaacataaa atgaatgcaa ttgttgttgt 2580taacttgttt attgcagctt
ataatggtta caaataaagc aatagcatca caaatttcac 2640aaataaagca
tttttttcac tgcattctag ttgtggtttg tccaaactca tcaatgtatc
2700ttatcatgtc ggcgcgttga cattgattat tgactagtta ttaatagtaa
tcaattacgg 2760ggtcattagt tcatagccca tatatggagt tccgcgttac
ataacttacg gtaaatggcc 2820cgcctggctg accgcccaac gacccccgcc
cattgacgtc aataatgacg tatgttccca 2880tagtaacgcc aatagggact
ttccattgac gtcaatgggt ggagtattta cggtaaactg 2940cccacttggc
agtacatcaa gtgtatcata tgccaagtac gccccctatt gacgtcaatg
3000acggtaaatg gcccgcctgg cattatgccc agtacatgac cttatgggac
tttcctactt 3060ggcagtacat ctacgtatta gtcatcgcta ttaccatggt
gatgcggttt tggcagtaca 3120tcaatgggcg tggatagcgg tttgactcac
ggggatttcc aagtctccac cccattgacg 3180tcaatgggag tttgttttgg
caccaaaatc aacgggactt tccaaaatgt cgtaacaact 3240ccgccccatt
gacgcaaatg ggcggtaggc gtgtacggtg ggaggtctat ataagcagag
3300ctctccctat cagtgataga gatctcccta tcagtgatag agatcgtcga
cgtttagtga 3360accgtcagat cgcctggaga cgccatccac gctgttttga
cctccataga agacaccggg 3420accgatccag cctccgcggc cgggaacggt
gcattggaac gcggattccc cgtgccaaga 3480gtgacgtaag taccgcctat
agagtctata ggcccacccc cttggcttct tatgcatgct 3540atactgtttt
tggcttgggg tctatacacc cccgcttcct catgttatag gtgatggtat
3600agcttagcct ataggtgtgg gttattgacc attattgacc actcccctat
tggtgacgat 3660actttccatt actaatccat aacatggctc tttgccacaa
ctctctttat tggctatatg 3720ccaatacact gtccttcaga gactgacacg
gactctgtat ttttacagga tggggtctca 3780tttattattt acaaattcac
atatacaaca ccaccgtccc cagtgcccgc agtttttatt 3840aaacataacg
tgggatctcc acgcgaatct cgggtacgtg ttccggacat ggtctcttct
3900ccggtagcgg cggagcttct acatccgagc cctgctccca tgcctccagc
gactcatggt 3960cgctcggcag ctccttgctc ctaacagtgg aggccagact
taggcacagc acgatgccca 4020ccaccaccag tgtgccgcac aaggccgtgg
cggtagggta tgtgtctgaa aatgagctcg 4080gggagcgggc ttgcaccgct
gacgcatttg gaagacttaa ggcagcggca gaagaagatg 4140caggcagctg
agttgttgtg ttctgataag agtcagaggt aactcccgtt gcggtgctgt
4200taacggtgga gggcagtgta gtctgagcag tactcgttgc tgccgcgcgc
gccaccagac 4260ataatagctg acagactaac agactgttcc tttccatggg
tcttttctgc agtcaccgtc 4320cttgacacga agcttatact cgagctctag
attgggaacc cgggtctctc gaattcgaga 4380tctccaccat gcacagacct
agacgtcgtg gaactcgtcc acctccactg gcactgctcg 4440ctgctctcct
cctggctgca cgtggtgctg atgcacaagt acaactgcaa caaagcggag
4500ctgaactggc caaaccaggc gcttccgtga agatgtcttg taaagccagc
gggtatacat 4560ttactaatta ctggattcac tgggagaagc aaagacctga
acagggattg gaatggattg 4620gatacattaa tcctaacacc ggacacacag
agtataatca aaaattcaag gataaggcca 4680ccctcacagc cgacagatct
tcttcaaccg cctatatgca actttcttcc ctcacttctg 4740aagactccgc
agtttacttt tgcgcacgaa cttattctgg aagctcccat ttcgactact
4800ggggtcaagg aacaacactg atcgtgtcta gcggcggcgg agggtccggc
gggggcggta 4860gcggtggcgg aggttctgat attgtcatga ctcaaacacc
tgtctctctg cctgtttcac 4920ttggagatca agctagcatt tcctgccgct
ctagtcaatc tctcgtccac aacaacggcg 4980atactttctt gcattggtat
ctgcagaaac caggtcagtc acctaaactg cttatataca 5040aagtctctaa
tagattctca ggggtgccag atcgattcag tggttctggg tccggtacag
5100attttacact caagatatcc agagtagaag cagaagatct gggcgtgtat
ttctgcagtc 5160aaacaacact tattcctcgt acttttggag gcggtacaaa
actggagatc aagcgtggag 5220gcggagggag tgttttgttt tatctggccg
ttgggataat gtttctcgta aatacagtac 5280tttgggtaac aataaggaag
gaactgaaga gaaagaaaaa atgggatctg gaaatatcat 5340tggacagtgg
acacgaaaaa aaagtcacat catcattgca agaagaccgg cacttggagg
5400aggaactgaa atgtcaagag caaaaagaag aacaactgca agaaggcgta
catagaaaag 5460aaccacaggg agcaacatag gcggccgcta atcagccata
ccacatttgt agaggtttta 5520cttgctttaa aaaacctccc acacctcccc
ctgaacctga aacataaaat gaatgcaatt 5580gttgttgtta acttgtttat
tgcagcttat aatggttaca aataaagcaa tagcatcaca 5640aatttcacaa
ataaagcatt tttttcactg cattctagtt gtggtttgtc caaactcatc
5700aatgtatctt atcatgtcta ccggtataac ttcgtataat gtatactata
cgaagttag 5759237627DNAartificial sequencesynthetic 23aagcttatac
tcgagctcta gattgggaac ccgggtctct cgaattcgag atctccacca 60tgcacagacc
tagacgtcgt ggaactcgtc cacctccact ggcactgctc gctgctctcc
120tcctggctgc acgtggtgct gatgcacaag tacaactgca acaaagcgga
gctgaactgg 180ccaaaccagg cgcttccgtg aagatgtctt gtaaagccag
cgggtataca tttactaatt 240actggattca ctgggagaag caaagacctg
aacagggatt ggaatggatt ggatacatta 300atcctaacac cggacacaca
gagtataatc aaaaattcaa ggataaggcc accctcacag 360ccgacagatc
ttcttcaacc gcctatatgc aactttcttc cctcacttct gaagactccg
420cagtttactt ttgcgcacga acttattctg gaagctccca tttcgactac
tggggtcaag 480gaacaacact gatcgtgtct agcggcggcg gagggtccgg
cgggggcggt agcggtggcg 540gaggttctga tattgtcatg actcaaacac
ctgtctctct gcctgtttca cttggagatc 600aagctagcat ttcctgccgc
tctagtcaat ctctcgtcca caacaacggc gatactttct 660tgcattggta
tctgcagaaa ccaggtcagt cacctaaact gcttatatac aaagtctcta
720atagattctc aggggtgcca gatcgattca gtggttctgg gtccggtaca
gattttacac 780tcaagatatc cagagtagaa gcagaagatc tgggcgtgta
tttctgcagt caaacaacac 840ttattcctcg tacttttgga ggcggtacaa
aactggagat caagcgtgga ggcggaggga 900gtgttttgtt ttatctggcc
gttgggataa tgtttctcgt aaatacagta ctttgggtaa 960caataaggaa
ggaactgaag agaaagaaaa aatgggatct ggaaatatca ttggacagtg
1020gacacgaaaa aaaagtcaca tcatcattgc aagaagaccg gcacttggag
gaggaactga 1080aatgtcaaga gcaaaaagaa gaacaactgc aagaaggcgt
acatagaaaa gaaccacagg 1140gagcaacata ggcggccgct aatcagccat
accacatttg tagaggtttt acttgcttta 1200aaaaacctcc cacacctccc
cctgaacctg aaacataaaa tgaatgcaat tgttgttgtt 1260aacttgttta
ttgcagctta taatggttac aaataaagca atagcatcac aaatttcaca
1320aataaagcat ttttttcact gcattctagt tgtggtttgt ccaaactcat
caatgtatct 1380tatcatgtct accggtataa cttcgtataa tgtatactat
acgaagttag ccggtagggc 1440ccctctcttc atgtgagcaa aaggccagca
aaaggccagg aaccgtaaaa aggccgcgtt 1500gctggcgttt ttccataggc
tccgcccccc tgacgagcat cacaaaaatc gacgctcaag 1560tcagaggtgg
cgaaacccga caggactata aagataccag gcgtttcccc ctggaagctc
1620cctcgtgcgc tctcctgttc cgaccctgcc gcttaccgga tacctgtccg
cctttctccc 1680ttcgggaagc gtggcgcttt ctcatagctc acgctgtagg
tatctcagtt cggtgtaggt 1740cgttcgctcc aagctgggct gtgtgcacga
accccccgtt cagcccgacc gctgcgcctt 1800atccggtaac tatcgtcttg
agtccaaccc ggtaagacac gacttatcgc cactggcagc 1860agccactggt
aacaggatta gcagagcgag gtatgtaggc ggtgctacag agttcttgaa
1920gtggtggcct aactacggct acactagaag aacagtattt ggtatctgcg
ctctgctgaa 1980gccagttacc ttcggaaaaa gagttggtag ctcttgatcc
ggcaaacaaa ccaccgctgg 2040tagcggtggt ttttttgttt gcaagcagca
gattacgcgc agaaaaaaag gatctcaaga 2100agatcctttg atcttttcta
cggggtctga cgctcagtgg aacgaaaact cacgttaagg 2160gattttggtc
atgggcgcgc ctcatactcc tgcaggcatg agattatcaa aaaggatctt
2220cacctagatc cttttaaatt aaaaatgaag ttttaaatca atctaaagta
tatatgagta 2280aacttggtct gacagttacc aatgcttaat cagtgaggca
cctatctcag cgatctgtct 2340atttcgttca tccatagttg cctgactccc
cgtcgtgtag ataactacga tacgggaggg 2400cttaccatct ggccccagtg
ctgcaatgat accgcgagac ccacgctcac cggctccaga 2460tttatcagca
ataaaccagc cagccggaag ggccgagcgc agaagtggtc ctgcaacttt
2520atccgcctcc atccagtcta ttaattgttg ccgggaagct agagtaagta
gttcgccagt 2580taatagtttg cgcaacgttg ttgccattgc tacaggcatc
gtggtgtcac gctcgtcgtt 2640tggtatggct tcattcagct ccggttccca
acgatcaagg cgagttacat gatcccccat 2700gttgtgcaaa aaagcggtta
gctccttcgg tcctccgatc gttgtcagaa gtaagttggc 2760cgcagtgtta
tcactcatgg ttatggcagc actgcataat tctcttactg tcatgccatc
2820cgtaagatgc ttttctgtga ctggtgagta ctcaaccaag tcattctgag
aatagtgtat 2880gcggcgaccg agttgctctt gcccggcgtc aatacgggat
aatactgcgc cacatagcag 2940aactttaaaa gtgctcatca ttggaaaacg
ttcttcgggg cgaaaactct caaggatctt 3000accgctgttg agatccagtt
cgatgtaacc cactcgtgca cccaactgat cttcagcatc 3060ttttactttc
accagcgttt ctgggtgagc aaaaacagga aggcaaaatg ccgcaaaaaa
3120gggaataagg gcgacacgga aatgttgaat actcatactc ttcctttttc
aatattattg 3180aagcatttat cagggttatt gtctcatgag cggatacata
tttgaatgta tttagaaaaa 3240taaacaaata ggggttccgc gcacatttcc
ccgaaaagtg ccacctgacg tcaggtacac 3300aacttcgtat agcatacatt
atacgaagtt atggtaccaa gcctaggcct ccaaaaaagc 3360ctcctcacta
cttctggaat agctcagagg cagaggcggc ctcggcctct gcataaataa
3420aaaaaattag tcagccatgg ggcggagaat gggcggaact gggcggagtt
aggggcggga 3480tgggcggagt taggggcggg actatggttg ctgactaatt
gagatgcatg ctttgcatac 3540ttctgcctgc tggggagcct ggggactttc
cacacctggt tgctgactaa ttgagatgca 3600tgctttgcat acttctgcct
gctggggagc ctggggactt tccacaccgg atccaccatg 3660ggttcagcta
ttgagcagga tgggttgcat gctggtagtc ccgccgcatg ggtcgaacga
3720ctgtttggat acgattgggc ccaacagact ataggctgtt ccgacgctgc
tgtctttcgt 3780ctttctgcac aaggtcgtcc agttctgttc gtgaaaaccg
acttgtccgg agccctcaat 3840gagttgcaag acgaagctgc acgactgagt
tggcttgcca ccactggtgt cccatgtgcc 3900gcagtacttg acgtcgtcac
agaggctggt cgcgattggt tgctccttgg agaagtgccc 3960ggccaagatc
ttctcagttc ccaccttgcc cctgccgaaa aagtttcaat aatggctgac
4020gctatgagaa ggctgcacac ccttgaccct gccacatgtc cattcgatca
ccaagccaaa 4080caccgaattg aacgagctag aacccgcatg gaagccggcc
tcgttgatca agacgatttg 4140gatgaggaac accagggtct cgcacccgct
gaactcttcg ctcgcctcaa agcacgaatg 4200ccagacggag atgacttggt
cgtaacccac ggagatgcct gccttcctaa cataatggta 4260gagaatggaa
gatttagcgg cttcattgat tgtggacgac ttggagttgc agatcggtac
4320caagatatcg ctctcgctac cagagatatt gctgaagaat tgggcggaga
atgggctgat 4380cggtttctcg tactctacgg aattgccgca cctgattccc
aacgcattgc tttttaccgt 4440cttctggatg agttcttcta aacgcgtccc
ccctctccct cccccccccc taacgttact 4500ggccgaagcc gcttggaata
aggccggtgt gcgtttgtct atatgttatt ttccaccata 4560ttgccgtctt
ttggcaatgt gagggcccgg aaacctggcc ctgtcttctt gacgagcatt
4620cctaggggtc tttcccctct cgccaaagga atgcaaggtc tgttgaatgt
cgtgaaggaa 4680gcagttcctc tggaagcttc ttgaagacaa acaacgtctg
tagcgaccct ttgcaggcag 4740cggaaccccc cacctggcga caggtgcctc
tgcggccaaa agccacgtgt ataagataca 4800cctgcaaagg cggcacaacc
ccagtgccac gttgtgagtt ggatagttgt ggaaagagtc 4860aaatggctct
cctcaagcgt attcaacaag gggctgaagg atgcccagaa ggtaccccat
4920tgtatgggat ctgatctggg gcctcggtgc acatgcttta catgtgttta
gtcgaggtta 4980aaaaacgtct aggccccccg aaccacgggg acgtggtttt
cctttgaaaa acacgattgc 5040tcgaatcacc atggtgagca agggcgagga
gctgttcacc ggggtggtgc ccatcctggt 5100cgagctggac ggcgacgtaa
acggccacaa gttcagcgtg tccggcgagg gcgagggcga 5160tgccacctac
ggcaagctga ccctgaagtt catctgcacc accggcaagc tgcccgtgcc
5220ctggcccacc ctcgtgacca ccttcggcta cggcctgcag tgcttcgccc
gctaccccga 5280ccacatgaag cagcacgact tcttcaagtc cgccatgccc
gaaggctacg tccaggagcg 5340caccatcttc ttcaaggacg acggcaacta
caagacccgc gccgaggtga agttcgaggg 5400cgacaccctg gtgaaccgca
tcgagctgaa gggcatcgac ttcaaggagg acggcaacat 5460cctggggcac
aagctggagt acaactacaa cagccacaac gtctatatca tggccgacaa
5520gcagaagaac ggcatcaagg tgaacttcaa gatccgccac aacatcgagg
acggcagcgt 5580gcagctcgcc gaccactacc agcagaacac ccccatcggc
gacggccccg tgctgctgcc 5640cgacaaccac tacctgagct accagtccgc
cctgagcaaa gaccccaacg agaagcgcga 5700tcacatggtc ctgctggagt
tcgtgaccgc cgccgggatc actctcggca tggacgagct 5760gtacaagtaa
tcggccgcta atcagccata ccacatttgt agaggtttta cttgctttaa
5820aaaacctccc acacctcccc ctgaacctga aacataaaat gaatgcaatt
gttgttgtta 5880acttgtttat tgcagcttat aatggttaca aataaagcaa
tagcatcaca aatttcacaa 5940ataaagcatt tttttcactg cattctagtt
gtggtttgtc caaactcatc aatgtatctt 6000atcatgtcgg cgcgttgaca
ttgattattg actagttatt aatagtaatc aattacgggg 6060tcattagttc
atagcccata tatggagttc cgcgttacat aacttacggt aaatggcccg
6120cctggctgac cgcccaacga cccccgccca ttgacgtcaa taatgacgta
tgttcccata 6180gtaacgccaa tagggacttt ccattgacgt caatgggtgg
agtatttacg gtaaactgcc 6240cacttggcag tacatcaagt gtatcatatg
ccaagtacgc cccctattga cgtcaatgac 6300ggtaaatggc ccgcctggca
ttatgcccag tacatgacct tatgggactt tcctacttgg 6360cagtacatct
acgtattagt catcgctatt accatggtga tgcggttttg gcagtacatc
6420aatgggcgtg gatagcggtt tgactcacgg ggatttccaa gtctccaccc
cattgacgtc 6480aatgggagtt tgttttggca ccaaaatcaa cgggactttc
caaaatgtcg taacaactcc 6540gccccattga cgcaaatggg cggtaggcgt
gtacggtggg aggtctatat aagcagagct 6600ctccctatca gtgatagaga
tctccctatc agtgatagag atcgtcgacg tttagtgaac 6660cgtcagatcg
cctggagacg ccatccacgc tgttttgacc tccatagaag acaccgggac
6720cgatccagcc tccgcggccg ggaacggtgc attggaacgc ggattccccg
tgccaagagt 6780gacgtaagta ccgcctatag agtctatagg cccaccccct
tggcttctta tgcatgctat 6840actgtttttg gcttggggtc tatacacccc
cgcttcctca tgttataggt gatggtatag 6900cttagcctat aggtgtgggt
tattgaccat tattgaccac tcccctattg gtgacgatac 6960tttccattac
taatccataa catggctctt tgccacaact ctctttattg gctatatgcc
7020aatacactgt ccttcagaga ctgacacgga ctctgtattt ttacaggatg
gggtctcatt 7080tattatttac aaattcacat atacaacacc accgtcccca
gtgcccgcag tttttattaa 7140acataacgtg ggatctccac gcgaatctcg
ggtacgtgtt ccggacatgg tctcttctcc 7200ggtagcggcg gagcttctac
atccgagccc tgctcccatg cctccagcga ctcatggtcg 7260ctcggcagct
ccttgctcct aacagtggag gccagactta ggcacagcac gatgcccacc
7320accaccagtg tgccgcacaa ggccgtggcg gtagggtatg tgtctgaaaa
tgagctcggg 7380gagcgggctt gcaccgctga cgcatttgga agacttaagg
cagcggcaga agaagatgca 7440ggcagctgag ttgttgtgtt ctgataagag
tcagaggtaa ctcccgttgc ggtgctgtta 7500acggtggagg gcagtgtagt
ctgagcagta ctcgttgctg ccgcgcgcgc caccagacat 7560aatagctgac
agactaacag actgttcctt tccatgggtc ttttctgcag tcaccgtcct 7620tgacacg
7627242669DNAartificial sequencesynthetic 24agcctaggcc tccaaaaaag
cctcctcact acttctggaa tagctcagag gcagaggcgg 60cctcggcctc tgcataaata
aaaaaaatta gtcagccatg gggcggagaa tgggcggaac 120tgggcggagt
taggggcggg atgggcggag ttaggggcgg gactatggtt gctgactaat
180tgagatgcat gctttgcata cttctgcctg ctggggagcc tggggacttt
ccacacctgg 240ttgctgacta attgagatgc atgctttgca tacttctgcc
tgctggggag cctggggact 300ttccacaccg gatccaccat gggttcagct
attgagcagg atgggttgca tgctggtagt 360cccgccgcat gggtcgaacg
actgtttgga tacgattggg cccaacagac tataggctgt 420tccgacgctg
ctgtctttcg tctttctgca caaggtcgtc cagttctgtt cgtgaaaacc
480gacttgtccg gagccctcaa tgagttgcaa gacgaagctg cacgactgag
ttggcttgcc 540accactggtg tcccatgtgc cgcagtactt gacgtcgtca
cagaggctgg tcgcgattgg 600ttgctccttg gagaagtgcc cggccaagat
cttctcagtt cccaccttgc ccctgccgaa 660aaagtttcaa taatggctga
cgctatgaga aggctgcaca cccttgaccc tgccacatgt 720ccattcgatc
accaagccaa acaccgaatt gaacgagcta gaacccgcat ggaagccggc
780ctcgttgatc aagacgattt ggatgaggaa caccagggtc tcgcacccgc
tgaactcttc 840gctcgcctca aagcacgaat gccagacgga gatgacttgg
tcgtaaccca cggagatgcc 900tgccttccta acataatggt agagaatgga
agatttagcg gcttcattga ttgtggacga 960cttggagttg cagatcggta
ccaagatatc gctctcgcta ccagagatat tgctgaagaa 1020ttgggcggag
aatgggctga tcggtttctc gtactctacg gaattgccgc acctgattcc
1080caacgcattg ctttttaccg tcttctggat gagttcttct aaacgcgtcc
cccctctccc 1140tccccccccc ctaacgttac tggccgaagc cgcttggaat
aaggccggtg tgcgtttgtc 1200tatatgttat tttccaccat attgccgtct
tttggcaatg tgagggcccg gaaacctggc 1260cctgtcttct tgacgagcat
tcctaggggt ctttcccctc tcgccaaagg aatgcaaggt 1320ctgttgaatg
tcgtgaagga agcagttcct ctggaagctt cttgaagaca aacaacgtct
1380gtagcgaccc tttgcaggca gcggaacccc ccacctggcg acaggtgcct
ctgcggccaa 1440aagccacgtg tataagatac acctgcaaag gcggcacaac
cccagtgcca cgttgtgagt 1500tggatagttg tggaaagagt caaatggctc
tcctcaagcg tattcaacaa ggggctgaag 1560gatgcccaga aggtacccca
ttgtatggga tctgatctgg ggcctcggtg cacatgcttt 1620acatgtgttt
agtcgaggtt aaaaaacgtc taggcccccc gaaccacggg gacgtggttt
1680tcctttgaaa aacacgattg ctcgaatcac catggtgagc aagggcgagg
agctgttcac 1740cggggtggtg cccatcctgg tcgagctgga cggcgacgta
aacggccaca agttcagcgt 1800gtccggcgag ggcgagggcg atgccaccta
cggcaagctg accctgaagt tcatctgcac 1860caccggcaag ctgcccgtgc
cctggcccac cctcgtgacc accttcggct acggcctgca 1920gtgcttcgcc
cgctaccccg accacatgaa gcagcacgac ttcttcaagt ccgccatgcc
1980cgaaggctac gtccaggagc gcaccatctt cttcaaggac gacggcaact
acaagacccg 2040cgccgaggtg aagttcgagg gcgacaccct ggtgaaccgc
atcgagctga agggcatcga 2100cttcaaggag gacggcaaca tcctggggca
caagctggag tacaactaca acagccacaa 2160cgtctatatc atggccgaca
agcagaagaa cggcatcaag gtgaacttca agatccgcca 2220caacatcgag
gacggcagcg tgcagctcgc cgaccactac cagcagaaca cccccatcgg
2280cgacggcccc gtgctgctgc ccgacaacca ctacctgagc taccagtccg
ccctgagcaa 2340agaccccaac gagaagcgcg atcacatggt cctgctggag
ttcgtgaccg ccgccgggat 2400cactctcggc atggacgagc tgtacaagta
atcggccgct aatcagccat accacatttg 2460tagaggtttt acttgcttta
aaaaacctcc cacacctccc cctgaacctg aaacataaaa 2520tgaatgcaat
tgttgttgtt aacttgttta ttgcagctta taatggttac aaataaagca
2580atagcatcac aaatttcaca aataaagcat ttttttcact gcattctagt
tgtggtttgt 2640ccaaactcat caatgtatct tatcatgtc
2669253003DNAartificial sequencesynthetic 25gttgacattg attattgact
agttattaat agtaatcaat tacggggtca ttagttcata 60gcccatatat ggagttccgc
gttacataac ttacggtaaa tggcccgcct ggctgaccgc 120ccaacgaccc
ccgcccattg acgtcaataa tgacgtatgt tcccatagta acgccaatag
180ggactttcca ttgacgtcaa tgggtggagt atttacggta aactgcccac
ttggcagtac 240atcaagtgta tcatatgcca agtacgcccc ctattgacgt
caatgacggt aaatggcccg 300cctggcatta tgcccagtac atgaccttat
gggactttcc tacttggcag tacatctacg 360tattagtcat cgctattacc
atggtgatgc ggttttggca gtacatcaat gggcgtggat 420agcggtttga
ctcacgggga tttccaagtc tccaccccat tgacgtcaat gggagtttgt
480tttggcacca aaatcaacgg gactttccaa aatgtcgtaa caactccgcc
ccattgacgc 540aaatgggcgg taggcgtgta cggtgggagg tctatataag
cagagctctc cctatcagtg 600atagagatct ccctatcagt gatagagatc
gtcgacgttt agtgaaccgt cagatcgcct 660ggagacgcca tccacgctgt
tttgacctcc atagaagaca ccgggaccga tccagcctcc 720gcggccggga
acggtgcatt ggaacgcgga ttccccgtgc caagagtgac gtaagtaccg
780cctatagagt ctataggccc acccccttgg cttcttatgc atgctatact
gtttttggct 840tggggtctat acacccccgc ttcctcatgt tataggtgat
ggtatagctt agcctatagg 900tgtgggttat tgaccattat tgaccactcc
cctattggtg acgatacttt ccattactaa 960tccataacat ggctctttgc
cacaactctc tttattggct atatgccaat acactgtcct 1020tcagagactg
acacggactc tgtattttta caggatgggg tctcatttat tatttacaaa
1080ttcacatata caacaccacc gtccccagtg cccgcagttt ttattaaaca
taacgtggga 1140tctccacgcg aatctcgggt acgtgttccg gacatggtct
cttctccggt agcggcggag 1200cttctacatc cgagccctgc tcccatgcct
ccagcgactc atggtcgctc ggcagctcct 1260tgctcctaac agtggaggcc
agacttaggc acagcacgat gcccaccacc accagtgtgc 1320cgcacaaggc
cgtggcggta gggtatgtgt ctgaaaatga gctcggggag cgggcttgca
1380ccgctgacgc atttggaaga cttaaggcag cggcagaaga agatgcaggc
agctgagttg 1440ttgtgttctg ataagagtca gaggtaactc ccgttgcggt
gctgttaacg gtggagggca 1500gtgtagtctg agcagtactc gttgctgccg
cgcgcgccac cagacataat agctgacaga 1560ctaacagact gttcctttcc
atgggtcttt tctgcagtca ccgtccttga cacgaagctt 1620atactcgagc
tctagattgg gaacccgggt ctctcgaatt cgagatctcc accatgcaca
1680gacctagacg tcgtggaact cgtccacctc cactggcact gctcgctgct
ctcctcctgg 1740ctgcacgtgg tgctgatgca caagtacaac tgcaacaaag
cggagctgaa ctggccaaac 1800caggcgcttc cgtgaagatg tcttgtaaag
ccagcgggta tacatttact aattactgga 1860ttcactggga gaagcaaaga
cctgaacagg gattggaatg gattggatac attaatccta 1920acaccggaca
cacagagtat aatcaaaaat tcaaggataa ggccaccctc acagccgaca
1980gatcttcttc aaccgcctat atgcaacttt cttccctcac ttctgaagac
tccgcagttt 2040acttttgcgc acgaacttat tctggaagct cccatttcga
ctactggggt caaggaacaa 2100cactgatcgt gtctagcggc ggcggagggt
ccggcggggg cggtagcggt ggcggaggtt 2160ctgatattgt catgactcaa
acacctgtct ctctgcctgt ttcacttgga gatcaagcta 2220gcatttcctg
ccgctctagt caatctctcg tccacaacaa cggcgatact ttcttgcatt
2280ggtatctgca gaaaccaggt cagtcaccta aactgcttat atacaaagtc
tctaatagat 2340tctcaggggt gccagatcga ttcagtggtt ctgggtccgg
tacagatttt acactcaaga 2400tatccagagt agaagcagaa gatctgggcg
tgtatttctg cagtcaaaca acacttattc 2460ctcgtacttt tggaggcggt
acaaaactgg agatcaagcg tggaggcgga gggagtgttt 2520tgttttatct
ggccgttggg ataatgtttc tcgtaaatac agtactttgg gtaacaataa
2580ggaaggaact gaagagaaag aaaaaatggg atctggaaat atcattggac
agtggacacg 2640aaaaaaaagt cacatcatca ttgcaagaag accggcactt
ggaggaggaa ctgaaatgtc 2700aagagcaaaa agaagaacaa ctgcaagaag
gcgtacatag aaaagaacca cagggagcaa 2760cataggcggc cgctaatcag
ccataccaca tttgtagagg ttttacttgc tttaaaaaac 2820ctcccacacc
tccccctgaa cctgaaacat aaaatgaatg caattgttgt tgttaacttg
2880tttattgcag cttataatgg ttacaaataa agcaatagca tcacaaattt
cacaaataaa 2940gcattttttt cactgcattc tagttgtggt ttgtccaaac
tcatcaatgt atcttatcat 3000gtc 300326208PRTHomo sapiens 26Val Phe
Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg 1 5 10 15
Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro 20
25 30 Glu Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn
Ala 35 40 45 Lys Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr
Arg Val Val 50 55 60 Ser Val Leu Thr Val Leu His Gln Asp Trp Leu
Asn Gly Lys Glu Tyr 65 70 75 80 Lys Cys Lys Val Ser Asn Lys Gly Leu
Pro Ser Ser Ile Glu Lys Thr 85 90 95 Ile Ser Lys Ala Lys Gly Gln
Pro Arg Glu Pro Gln Val Tyr Thr Leu 100 105 110 Pro Pro Ser Gln Glu
Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys 115 120 125 Leu Val Lys
Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser 130 135 140 Asn
Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp 145 150
155 160 Ser Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys
Ser 165 170 175 Arg Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met
His Glu Ala 180 185 190 Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser
Leu Ser Leu Gly Lys 195 200 205 278PRTHomo sapiens 27Gly Tyr Thr
Phe Thr Asn Tyr Trp 1 5 288PRTHomo sapiens 28Ile Asn Pro Asn Thr
Gly His Thr 1 5 2913PRTHomo sapiens 29Cys Ala Arg Thr Tyr Ser Gly
Ser Ser His Phe Asp Tyr 1 5 10 3010PRTHomo sapiens 30Ser Leu Val
His Asn Asn Gly Asp Thr Phe 1 5 10 319PRTHomo sapiens 31Ser Gln Thr
Thr Leu Ile Pro Arg Thr 1
5 328PRTHomo sapiens 32Gly Phe Thr Phe Ser Asn Ala Trp 1 5
3310PRTHomo sapiens 33Ile Leu Ser Lys Thr Asp Gly Gly Thr Thr 1 5
10 3413PRTHomo sapiens 34Thr Thr Ala Asp Phe Trp Ser Ala Tyr Ser
Ser Asp Tyr 1 5 10 354PRTHomo sapiens 35Gln Ser Leu Leu 1
367PRTHomo sapiens 36His Ser Asn Gly Tyr Asn Tyr 1 5 379PRTHomo
sapiens 37Met Gln Gly Leu Gln Thr Pro Tyr Thr 1 5 38122PRTHomo
sapiens 38Glu Val Gln Leu Val Glu Ser Gly Gly Ala Ile Val Lys Pro
Gly Gly 1 5 10 15 Ser His Arg Val Ser Cys Glu Ala Ser Gly Phe Thr
Phe Ser Asn Ala 20 25 30 Trp Met Ser Trp Val Arg Gln Ala Pro Gly
Arg Gly Leu Glu Trp Val 35 40 45 Gly Arg Ile Leu Ser Lys Thr Asp
Gly Gly Thr Thr Asp Tyr Ala Ala 50 55 60 Pro Val Lys Asp Arg Phe
Thr Ile Ser Arg Asp Asp Ser Lys Asn Met 65 70 75 80 Leu Phe Leu Gln
Met Asp Ser Leu Lys Ile Glu Asp Thr Ala Val Tyr 85 90 95 Phe Cys
Thr Thr Ala Asp Phe Trp Ser Ala Tyr Ser Ser Asp Tyr Trp 100 105 110
Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 39112PRTHomo
sapiens 39Asp Ile Val Met Thr Gln Ser Pro Leu Ser Leu Pro Val Thr
Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser Cys Arg Ser Ser Gln Ser
Leu Leu His Ser 20 25 30 Asn Gly Tyr Asn Tyr Leu Asp Trp Tyr Leu
Gln Lys Pro Gly Gln Ser 35 40 45 Pro Gln Leu Leu Ile Tyr Leu Gly
Ser Asn Arg Ala Ser Gly Val Pro 50 55 60 Asp Arg Phe Ser Gly Ser
Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile 65 70 75 80 Ser Arg Met Glu
Ala Glu Asp Val Gly Val Tyr Tyr Cys Met Gln Gly 85 90 95 Leu Gln
Thr Pro Tyr Thr Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys 100 105 110
40452PRTHomo sapiens 40Glu Val Gln Leu Val Glu Ser Gly Gly Ala Ile
Val Lys Pro Gly Gly 1 5 10 15 Ser His Arg Val Ser Cys Glu Ala Ser
Gly Phe Thr Phe Ser Asn Ala 20 25 30 Trp Met Ser Trp Val Arg Gln
Ala Pro Gly Arg Gly Leu Glu Trp Val 35 40 45 Gly Arg Ile Leu Ser
Lys Thr Asp Gly Gly Thr Thr Asp Tyr Ala Ala 50 55 60 Pro Val Lys
Asp Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Met 65 70 75 80 Leu
Phe Leu Gln Met Asp Ser Leu Lys Ile Glu Asp Thr Ala Val Tyr 85 90
95 Phe Cys Thr Thr Ala Asp Phe Trp Ser Ala Tyr Ser Ser Asp Tyr Trp
100 105 110 Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Lys Thr Thr
Ala Pro 115 120 125 Ser Val Tyr Pro Leu Ala Pro Val Cys Gly Asp Thr
Thr Gly Ser Ser 130 135 140 Val Thr Leu Gly Cys Leu Val Lys Gly Tyr
Phe Pro Glu Pro Val Thr 145 150 155 160 Leu Thr Trp Asn Ser Gly Ser
Leu Ser Ser Gly Val His Thr Phe Pro 165 170 175 Ala Val Leu Gln Ser
Asp Leu Tyr Thr Leu Ser Ser Ser Val Thr Val 180 185 190 Thr Ser Ser
Thr Trp Pro Ser Gln Ser Ile Thr Cys Asn Val Ala His 195 200 205 Pro
Ala Ser Ser Thr Lys Val Asp Lys Lys Ile Glu Pro Arg Gly Pro 210 215
220 Thr Ile Lys Pro Cys Pro Pro Cys Lys Cys Pro Ala Pro Asn Leu Leu
225 230 235 240 Gly Gly Pro Ser Val Phe Ile Phe Pro Pro Lys Ile Lys
Asp Val Leu 245 250 255 Met Ile Ser Leu Ser Pro Ile Val Thr Cys Val
Val Val Asp Val Ser 260 265 270 Glu Asp Asp Pro Asp Val Gln Ile Ser
Trp Phe Val Asn Asn Val Glu 275 280 285 Val His Thr Ala Gln Thr Gln
Thr His Arg Glu Asp Tyr Asn Ser Thr 290 295 300 Leu Arg Val Val Ser
Ala Leu Pro Ile Gln His Gln Asp Trp Met Ser 305 310 315 320 Gly Lys
Glu Phe Lys Cys Lys Val Asn Asn Lys Asp Leu Pro Ala Pro 325 330 335
Ile Glu Arg Thr Ile Ser Lys Pro Lys Gly Ser Val Arg Ala Pro Gln 340
345 350 Val Tyr Val Leu Pro Pro Pro Glu Glu Glu Met Thr Lys Lys Gln
Val 355 360 365 Thr Leu Thr Cys Met Val Thr Asp Phe Met Pro Glu Asp
Ile Tyr Val 370 375 380 Glu Trp Thr Asn Asn Gly Lys Thr Glu Leu Asn
Tyr Lys Asn Thr Glu 385 390 395 400 Pro Val Leu Asp Ser Asp Gly Ser
Tyr Phe Met Tyr Ser Lys Leu Arg 405 410 415 Val Glu Lys Lys Asn Trp
Val Glu Arg Asn Ser Tyr Ser Cys Ser Val 420 425 430 Val His Glu Gly
Leu His Asn His His Thr Thr Lys Ser Phe Ser Arg 435 440 445 Thr Pro
Gly Lys 450 41219PRTHomo sapiens 41Asp Ile Val Met Thr Gln Ser Pro
Leu Ser Leu Pro Val Thr Pro Gly 1 5 10 15 Glu Pro Ala Ser Ile Ser
Cys Arg Ser Ser Gln Ser Leu Leu His Ser 20 25 30 Asn Gly Tyr Asn
Tyr Leu Asp Trp Tyr Leu Gln Lys Pro Gly Gln Ser 35 40 45 Pro Gln
Leu Leu Ile Tyr Leu Gly Ser Asn Arg Ala Ser Gly Val Pro 50 55 60
Asp Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Lys Ile 65
70 75 80 Ser Arg Met Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Met
Gln Gly 85 90 95 Leu Gln Thr Pro Tyr Thr Phe Gly Gln Gly Thr Lys
Leu Glu Ile Lys 100 105 110 Arg Ala Asp Ala Ala Pro Thr Val Ser Ile
Phe Pro Pro Ser Ser Glu 115 120 125 Gln Leu Thr Ser Gly Gly Ala Ser
Val Val Cys Phe Leu Asn Asn Phe 130 135 140 Tyr Pro Lys Asp Ile Asn
Val Lys Trp Lys Ile Asp Gly Ser Glu Arg 145 150 155 160 Gln Asn Gly
Val Leu Asn Ser Trp Thr Asp Gln Asp Ser Lys Asp Ser 165 170 175 Thr
Tyr Ser Met Ser Ser Thr Leu Thr Leu Thr Lys Asp Glu Tyr Glu 180 185
190 Arg His Asn Ser Tyr Thr Cys Glu Ala Thr His Lys Thr Ser Thr Ser
195 200 205 Pro Ile Val Lys Ser Phe Asn Arg Gly Glu Cys 210 215
42256PRTHomo sapiens 42Met Val Ser Tyr Trp Asp Thr Gly Val Leu Leu
Cys Ala Leu Leu Ser 1 5 10 15 Cys Leu Leu Leu Thr Gly Ser Ser Ser
Gly Gly Pro Gly Asp Lys Thr 20 25 30 His Thr Cys Pro Pro Cys Pro
Ala Pro Glu Leu Leu Gly Gly Pro Ser 35 40 45 Val Phe Leu Phe Pro
Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg 50 55 60 Thr Pro Glu
Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro 65 70 75 80 Glu
Val Lys Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala 85 90
95 Lys Thr Lys Pro Arg Glu Glu Gln Tyr Asn Ser Thr Tyr Arg Val Val
100 105 110 Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys
Glu Tyr 115 120 125 Lys Cys Lys Val Ser Asn Lys Ala Leu Pro Ala Pro
Ile Glu Lys Thr 130 135 140 Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu
Pro Gln Val Tyr Thr Leu 145 150 155 160 Pro Pro Ser Arg Asp Glu Leu
Thr Lys Asn Gln Val Ser Leu Thr Cys 165 170 175 Leu Val Lys Gly Phe
Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser 180 185 190 Asn Gly Gln
Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp 195 200 205 Ser
Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser 210 215
220 Arg Trp Gln Gln Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala
225 230 235 240 Leu His Asn Arg Phe Thr Gln Lys Ser Leu Ser Leu Ser
Pro Gly Lys 245 250 255 43336PRTArtificial sequencesynthetic 43Glu
Val Gln Leu Val Glu Ser Gly Gly Ala Ile Val Lys Pro Gly Gly 1 5 10
15 Ser His Arg Val Ser Cys Glu Ala Ser Gly Phe Thr Phe Ser Asn Ala
20 25 30 Trp Met Ser Trp Val Arg Gln Ala Pro Gly Arg Gly Leu Glu
Trp Val 35 40 45 Gly Arg Ile Leu Ser Lys Thr Asp Gly Gly Thr Thr
Asp Tyr Ala Ala 50 55 60 Pro Val Lys Asp Arg Phe Thr Ile Ser Arg
Asp Asp Ser Lys Asn Met 65 70 75 80 Leu Phe Leu Gln Met Asp Ser Leu
Lys Ile Glu Asp Thr Ala Val Tyr 85 90 95 Phe Cys Thr Thr Ala Asp
Phe Trp Ser Ala Tyr Ser Ser Asp Tyr Trp 100 105 110 Gly Gln Gly Thr
Leu Val Thr Val Ser Ser Gly Gly Gly Gly Ser Gly 115 120 125 Gly Gly
Gly Ser Gly Gly Gly Gly Ser Asp Ile Val Met Thr Gln Ser 130 135 140
Pro Leu Ser Leu Pro Val Thr Pro Gly Glu Pro Ala Ser Ile Ser Cys 145
150 155 160 Arg Ser Ser Gln Ser Leu Leu His Ser Asn Gly Tyr Asn Tyr
Leu Asp 165 170 175 Trp Tyr Leu Gln Lys Pro Gly Gln Ser Pro Gln Leu
Leu Ile Tyr Leu 180 185 190 Gly Ser Asn Arg Ala Ser Gly Val Pro Asp
Arg Phe Ser Gly Ser Gly 195 200 205 Ser Gly Thr Asp Phe Thr Leu Lys
Ile Ser Arg Met Glu Ala Glu Asp 210 215 220 Val Gly Val Tyr Tyr Cys
Met Gln Gly Leu Gln Thr Pro Tyr Thr Phe 225 230 235 240 Gly Gln Gly
Thr Lys Leu Glu Ile Lys Gly Gly Gly Gly Ser Val Leu 245 250 255 Phe
Tyr Leu Ala Val Gly Ile Met Phe Leu Val Asn Thr Val Leu Trp 260 265
270 Val Thr Ile Arg Lys Glu Leu Lys Arg Lys Lys Lys Trp Asp Leu Glu
275 280 285 Ile Ser Leu Asp Ser Gly His Glu Lys Lys Val Thr Ser Ser
Leu Gln 290 295 300 Glu Asp Arg His Leu Glu Glu Glu Leu Lys Cys Gln
Glu Gln Lys Glu 305 310 315 320 Glu Gln Leu Gln Glu Gly Val His Arg
Lys Glu Pro Gln Gly Ala Thr 325 330 335 447633DNAArtificial
sequencesynthetic 44aagcttatac tcgagctcta gattgggaac ccgggtctct
cgaattcgag atctccacca 60tgcacagacc tagacgtcgt ggaactcgtc cacctccact
ggcactgctc gctgctctcc 120tcctggctgc acgtggtgct gatgcagagg
tgcagctggt ggagtctggg ggagccatag 180taaagccggg ggggtcccat
agagtctcct gtgaagcctc tggattcact ttcagtaacg 240cctggatgag
ttgggtccgc caggctccag ggagggggct ggagtgggtt ggccgtattt
300taagcaagac tgatggtggg acgacagact acgctgcacc cgtgaaagac
agattcacca 360tttcaagaga tgattctaaa aatatgttgt ttctgcaaat
ggacagcctg aaaatcgagg 420acacagccgt gtatttctgt accacggccg
atttttggag tgcttattct tctgactact 480ggggccaggg aaccctggtc
accgtctcct caggaggtgg aggttccggg ggcgggggct 540ccggcggagg
tggatcagat attgtgatga ctcagtctcc actctccctg cccgtcaccc
600ctggagagcc ggcctccatc tcctgcaggt ctagtcagag cctcctgcat
agtaatgggt 660acaactattt ggattggtac ctacagaagc cagggcagtc
tccacaactc ctgatctatt 720tgggttctaa tcgggcctcc ggggtccctg
acaggttcag tggcagtgga tcaggcacag 780attttacact gaaaatcagc
agaatggagg ctgaggatgt tggggtttat tactgcatgc 840aaggtctaca
aactccgtac acttttggcc aggggaccaa gctggagatc aaaggaggcg
900gagggagtgt tttgttttat ctggccgttg ggataatgtt tctcgtaaat
acagtacttt 960gggtaacaat aaggaaggaa ctgaagagaa agaaaaaatg
ggatctggaa atatcattgg 1020acagtggaca cgaaaaaaaa gtcacatcat
cattgcaaga agaccggcac ttggaggagg 1080aactgaaatg tcaagagcaa
aaagaagaac aactgcaaga aggcgtacat agaaaagaac 1140cacagggagc
aacataggcg gccgctaatc agccatacca catttgtaga ggttttactt
1200gctttaaaaa acctcccaca cctccccctg aacctgaaac ataaaatgaa
tgcaattgtt 1260gttgttaact tgtttattgc agcttataat ggttacaaat
aaagcaatag catcacaaat 1320ttcacaaata aagcattttt ttcactgcat
tctagttgtg gtttgtccaa actcatcaat 1380gtatcttatc atgtctaccg
gtataacttc gtataatgta tactatacga agttagccgg 1440tagggcccct
ctcttcatgt gagcaaaagg ccagcaaaag gccaggaacc gtaaaaaggc
1500cgcgttgctg gcgtttttcc ataggctccg cccccctgac gagcatcaca
aaaatcgacg 1560ctcaagtcag aggtggcgaa acccgacagg actataaaga
taccaggcgt ttccccctgg 1620aagctccctc gtgcgctctc ctgttccgac
cctgccgctt accggatacc tgtccgcctt 1680tctcccttcg ggaagcgtgg
cgctttctca tagctcacgc tgtaggtatc tcagttcggt 1740gtaggtcgtt
cgctccaagc tgggctgtgt gcacgaaccc cccgttcagc ccgaccgctg
1800cgccttatcc ggtaactatc gtcttgagtc caacccggta agacacgact
tatcgccact 1860ggcagcagcc actggtaaca ggattagcag agcgaggtat
gtaggcggtg ctacagagtt 1920cttgaagtgg tggcctaact acggctacac
tagaagaaca gtatttggta tctgcgctct 1980gctgaagcca gttaccttcg
gaaaaagagt tggtagctct tgatccggca aacaaaccac 2040cgctggtagc
ggtggttttt ttgtttgcaa gcagcagatt acgcgcagaa aaaaaggatc
2100tcaagaagat cctttgatct tttctacggg gtctgacgct cagtggaacg
aaaactcacg 2160ttaagggatt ttggtcatgg gcgcgcctca tactcctgca
ggcatgagat tatcaaaaag 2220gatcttcacc tagatccttt taaattaaaa
atgaagtttt aaatcaatct aaagtatata 2280tgagtaaact tggtctgaca
gttaccaatg cttaatcagt gaggcaccta tctcagcgat 2340ctgtctattt
cgttcatcca tagttgcctg actccccgtc gtgtagataa ctacgatacg
2400ggagggctta ccatctggcc ccagtgctgc aatgataccg cgagacccac
gctcaccggc 2460tccagattta tcagcaataa accagccagc cggaagggcc
gagcgcagaa gtggtcctgc 2520aactttatcc gcctccatcc agtctattaa
ttgttgccgg gaagctagag taagtagttc 2580gccagttaat agtttgcgca
acgttgttgc cattgctaca ggcatcgtgg tgtcacgctc 2640gtcgtttggt
atggcttcat tcagctccgg ttcccaacga tcaaggcgag ttacatgatc
2700ccccatgttg tgcaaaaaag cggttagctc cttcggtcct ccgatcgttg
tcagaagtaa 2760gttggccgca gtgttatcac tcatggttat ggcagcactg
cataattctc ttactgtcat 2820gccatccgta agatgctttt ctgtgactgg
tgagtactca accaagtcat tctgagaata 2880gtgtatgcgg cgaccgagtt
gctcttgccc ggcgtcaata cgggataata ctgcgccaca 2940tagcagaact
ttaaaagtgc tcatcattgg aaaacgttct tcggggcgaa aactctcaag
3000gatcttaccg ctgttgagat ccagttcgat gtaacccact cgtgcaccca
actgatcttc 3060agcatctttt actttcacca gcgtttctgg gtgagcaaaa
acaggaaggc aaaatgccgc 3120aaaaaaggga ataagggcga cacggaaatg
ttgaatactc atactcttcc tttttcaata 3180ttattgaagc atttatcagg
gttattgtct catgagcgga tacatatttg aatgtattta 3240gaaaaataaa
caaatagggg ttccgcgcac atttccccga aaagtgccac ctgacgtcag
3300gtacacaact tcgtatagca tacattatac gaagttatgg taccaagcct
aggcctccaa 3360aaaagcctcc tcactacttc tggaatagct cagaggcaga
ggcggcctcg gcctctgcat 3420aaataaaaaa aattagtcag ccatggggcg
gagaatgggc ggaactgggc ggagttaggg 3480gcgggatggg cggagttagg
ggcgggacta tggttgctga ctaattgaga tgcatgcttt 3540gcatacttct
gcctgctggg gagcctgggg actttccaca cctggttgct gactaattga
3600gatgcatgct ttgcatactt ctgcctgctg gggagcctgg ggactttcca
caccggatcc 3660accatgggtt cagctattga gcaggatggg ttgcatgctg
gtagtcccgc cgcatgggtc 3720gaacgactgt ttggatacga ttgggcccaa
cagactatag gctgttccga cgctgctgtc 3780tttcgtcttt ctgcacaagg
tcgtccagtt ctgttcgtga aaaccgactt gtccggagcc 3840ctcaatgagt
tgcaagacga agctgcacga ctgagttggc ttgccaccac tggtgtccca
3900tgtgccgcag tacttgacgt cgtcacagag gctggtcgcg attggttgct
ccttggagaa 3960gtgcccggcc aagatcttct cagttcccac cttgcccctg
ccgaaaaagt ttcaataatg 4020gctgacgcta tgagaaggct gcacaccctt
gaccctgcca catgtccatt cgatcaccaa 4080gccaaacacc gaattgaacg
agctagaacc cgcatggaag ccggcctcgt tgatcaagac 4140gatttggatg
aggaacacca gggtctcgca cccgctgaac tcttcgctcg cctcaaagca
4200cgaatgccag acggagatga cttggtcgta acccacggag atgcctgcct
tcctaacata 4260atggtagaga atggaagatt tagcggcttc attgattgtg
gacgacttgg agttgcagat 4320cggtaccaag atatcgctct cgctaccaga
gatattgctg aagaattggg cggagaatgg 4380gctgatcggt ttctcgtact
ctacggaatt gccgcacctg attcccaacg cattgctttt 4440taccgtcttc
tggatgagtt cttctaaacg cgtcccccct ctccctcccc cccccctaac
4500gttactggcc gaagccgctt ggaataaggc cggtgtgcgt ttgtctatat
gttattttcc 4560accatattgc cgtcttttgg caatgtgagg gcccggaaac
ctggccctgt cttcttgacg 4620agcattccta
ggggtctttc ccctctcgcc aaaggaatgc aaggtctgtt gaatgtcgtg
4680aaggaagcag ttcctctgga agcttcttga agacaaacaa cgtctgtagc
gaccctttgc 4740aggcagcgga accccccacc tggcgacagg tgcctctgcg
gccaaaagcc acgtgtataa 4800gatacacctg caaaggcggc acaaccccag
tgccacgttg tgagttggat agttgtggaa 4860agagtcaaat ggctctcctc
aagcgtattc aacaaggggc tgaaggatgc ccagaaggta 4920ccccattgta
tgggatctga tctggggcct cggtgcacat gctttacatg tgtttagtcg
4980aggttaaaaa acgtctaggc cccccgaacc acggggacgt ggttttcctt
tgaaaaacac 5040gattgctcga atcaccatgg tgagcaaggg cgaggagctg
ttcaccgggg tggtgcccat 5100cctggtcgag ctggacggcg acgtaaacgg
ccacaagttc agcgtgtccg gcgagggcga 5160gggcgatgcc acctacggca
agctgaccct gaagttcatc tgcaccaccg gcaagctgcc 5220cgtgccctgg
cccaccctcg tgaccacctt cggctacggc ctgcagtgct tcgcccgcta
5280ccccgaccac atgaagcagc acgacttctt caagtccgcc atgcccgaag
gctacgtcca 5340ggagcgcacc atcttcttca aggacgacgg caactacaag
acccgcgccg aggtgaagtt 5400cgagggcgac accctggtga accgcatcga
gctgaagggc atcgacttca aggaggacgg 5460caacatcctg gggcacaagc
tggagtacaa ctacaacagc cacaacgtct atatcatggc 5520cgacaagcag
aagaacggca tcaaggtgaa cttcaagatc cgccacaaca tcgaggacgg
5580cagcgtgcag ctcgccgacc actaccagca gaacaccccc atcggcgacg
gccccgtgct 5640gctgcccgac aaccactacc tgagctacca gtccgccctg
agcaaagacc ccaacgagaa 5700gcgcgatcac atggtcctgc tggagttcgt
gaccgccgcc gggatcactc tcggcatgga 5760cgagctgtac aagtaatcgg
ccgctaatca gccataccac atttgtagag gttttacttg 5820ctttaaaaaa
cctcccacac ctccccctga acctgaaaca taaaatgaat gcaattgttg
5880ttgttaactt gtttattgca gcttataatg gttacaaata aagcaatagc
atcacaaatt 5940tcacaaataa agcatttttt tcactgcatt ctagttgtgg
tttgtccaaa ctcatcaatg 6000tatcttatca tgtcggcgcg ttgacattga
ttattgacta gttattaata gtaatcaatt 6060acggggtcat tagttcatag
cccatatatg gagttccgcg ttacataact tacggtaaat 6120ggcccgcctg
gctgaccgcc caacgacccc cgcccattga cgtcaataat gacgtatgtt
6180cccatagtaa cgccaatagg gactttccat tgacgtcaat gggtggagta
tttacggtaa 6240actgcccact tggcagtaca tcaagtgtat catatgccaa
gtacgccccc tattgacgtc 6300aatgacggta aatggcccgc ctggcattat
gcccagtaca tgaccttatg ggactttcct 6360acttggcagt acatctacgt
attagtcatc gctattacca tggtgatgcg gttttggcag 6420tacatcaatg
ggcgtggata gcggtttgac tcacggggat ttccaagtct ccaccccatt
6480gacgtcaatg ggagtttgtt ttggcaccaa aatcaacggg actttccaaa
atgtcgtaac 6540aactccgccc cattgacgca aatgggcggt aggcgtgtac
ggtgggaggt ctatataagc 6600agagctctcc ctatcagtga tagagatctc
cctatcagtg atagagatcg tcgacgttta 6660gtgaaccgtc agatcgcctg
gagacgccat ccacgctgtt ttgacctcca tagaagacac 6720cgggaccgat
ccagcctccg cggccgggaa cggtgcattg gaacgcggat tccccgtgcc
6780aagagtgacg taagtaccgc ctatagagtc tataggccca cccccttggc
ttcttatgca 6840tgctatactg tttttggctt ggggtctata cacccccgct
tcctcatgtt ataggtgatg 6900gtatagctta gcctataggt gtgggttatt
gaccattatt gaccactccc ctattggtga 6960cgatactttc cattactaat
ccataacatg gctctttgcc acaactctct ttattggcta 7020tatgccaata
cactgtcctt cagagactga cacggactct gtatttttac aggatggggt
7080ctcatttatt atttacaaat tcacatatac aacaccaccg tccccagtgc
ccgcagtttt 7140tattaaacat aacgtgggat ctccacgcga atctcgggta
cgtgttccgg acatggtctc 7200ttctccggta gcggcggagc ttctacatcc
gagccctgct cccatgcctc cagcgactca 7260tggtcgctcg gcagctcctt
gctcctaaca gtggaggcca gacttaggca cagcacgatg 7320cccaccacca
ccagtgtgcc gcacaaggcc gtggcggtag ggtatgtgtc tgaaaatgag
7380ctcggggagc gggcttgcac cgctgacgca tttggaagac ttaaggcagc
ggcagaagaa 7440gatgcaggca gctgagttgt tgtgttctga taagagtcag
aggtaactcc cgttgcggtg 7500ctgttaacgg tggagggcag tgtagtctga
gcagtactcg ttgctgccgc gcgcgccacc 7560agacataata gctgacagac
taacagactg ttcctttcca tgggtctttt ctgcagtcac 7620cgtccttgac acg
7633451011DNAArtificial sequencesynthetic 45gaggtgcagc tggtggagtc
tgggggagcc atagtaaagc cgggggggtc ccatagagtc 60tcctgtgaag cctctggatt
cactttcagt aacgcctgga tgagttgggt ccgccaggct 120ccagggaggg
ggctggagtg ggttggccgt attttaagca agactgatgg tgggacgaca
180gactacgctg cacccgtgaa agacagattc accatttcaa gagatgattc
taaaaatatg 240ttgtttctgc aaatggacag cctgaaaatc gaggacacag
ccgtgtattt ctgtaccacg 300gccgattttt ggagtgctta ttcttctgac
tactggggcc agggaaccct ggtcaccgtc 360tcctcaggag gtggaggttc
cgggggcggg ggctccggcg gaggtggatc agatattgtg 420atgactcagt
ctccactctc cctgcccgtc acccctggag agccggcctc catctcctgc
480aggtctagtc agagcctcct gcatagtaat gggtacaact atttggattg
gtacctacag 540aagccagggc agtctccaca actcctgatc tatttgggtt
ctaatcgggc ctccggggtc 600cctgacaggt tcagtggcag tggatcaggc
acagatttta cactgaaaat cagcagaatg 660gaggctgagg atgttggggt
ttattactgc atgcaaggtc tacaaactcc gtacactttt 720ggccagggga
ccaagctgga gatcaaagga ggcggaggga gtgttttgtt ttatctggcc
780gttgggataa tgtttctcgt aaatacagta ctttgggtaa caataaggaa
ggaactgaag 840agaaagaaaa aatgggatct ggaaatatca ttggacagtg
gacacgaaaa aaaagtcaca 900tcatcattgc aagaagaccg gcacttggag
gaggaactga aatgtcaaga gcaaaaagaa 960gaacaactgc aagaaggcgt
acatagaaaa gaaccacagg gagcaacata g 1011462669DNAArtificial
sequencesynthetic 46agcctaggcc tccaaaaaag cctcctcact acttctggaa
tagctcagag gcagaggcgg 60cctcggcctc tgcataaata aaaaaaatta gtcagccatg
gggcggagaa tgggcggaac 120tgggcggagt taggggcggg atgggcggag
ttaggggcgg gactatggtt gctgactaat 180tgagatgcat gctttgcata
cttctgcctg ctggggagcc tggggacttt ccacacctgg 240ttgctgacta
attgagatgc atgctttgca tacttctgcc tgctggggag cctggggact
300ttccacaccg gatccaccat gggttcagct attgagcagg atgggttgca
tgctggtagt 360cccgccgcat gggtcgaacg actgtttgga tacgattggg
cccaacagac tataggctgt 420tccgacgctg ctgtctttcg tctttctgca
caaggtcgtc cagttctgtt cgtgaaaacc 480gacttgtccg gagccctcaa
tgagttgcaa gacgaagctg cacgactgag ttggcttgcc 540accactggtg
tcccatgtgc cgcagtactt gacgtcgtca cagaggctgg tcgcgattgg
600ttgctccttg gagaagtgcc cggccaagat cttctcagtt cccaccttgc
ccctgccgaa 660aaagtttcaa taatggctga cgctatgaga aggctgcaca
cccttgaccc tgccacatgt 720ccattcgatc accaagccaa acaccgaatt
gaacgagcta gaacccgcat ggaagccggc 780ctcgttgatc aagacgattt
ggatgaggaa caccagggtc tcgcacccgc tgaactcttc 840gctcgcctca
aagcacgaat gccagacgga gatgacttgg tcgtaaccca cggagatgcc
900tgccttccta acataatggt agagaatgga agatttagcg gcttcattga
ttgtggacga 960cttggagttg cagatcggta ccaagatatc gctctcgcta
ccagagatat tgctgaagaa 1020ttgggcggag aatgggctga tcggtttctc
gtactctacg gaattgccgc acctgattcc 1080caacgcattg ctttttaccg
tcttctggat gagttcttct aaacgcgtcc cccctctccc 1140tccccccccc
ctaacgttac tggccgaagc cgcttggaat aaggccggtg tgcgtttgtc
1200tatatgttat tttccaccat attgccgtct tttggcaatg tgagggcccg
gaaacctggc 1260cctgtcttct tgacgagcat tcctaggggt ctttcccctc
tcgccaaagg aatgcaaggt 1320ctgttgaatg tcgtgaagga agcagttcct
ctggaagctt cttgaagaca aacaacgtct 1380gtagcgaccc tttgcaggca
gcggaacccc ccacctggcg acaggtgcct ctgcggccaa 1440aagccacgtg
tataagatac acctgcaaag gcggcacaac cccagtgcca cgttgtgagt
1500tggatagttg tggaaagagt caaatggctc tcctcaagcg tattcaacaa
ggggctgaag 1560gatgcccaga aggtacccca ttgtatggga tctgatctgg
ggcctcggtg cacatgcttt 1620acatgtgttt agtcgaggtt aaaaaacgtc
taggcccccc gaaccacggg gacgtggttt 1680tcctttgaaa aacacgattg
ctcgaatcac catggtgagc aagggcgagg agctgttcac 1740cggggtggtg
cccatcctgg tcgagctgga cggcgacgta aacggccaca agttcagcgt
1800gtccggcgag ggcgagggcg atgccaccta cggcaagctg accctgaagt
tcatctgcac 1860caccggcaag ctgcccgtgc cctggcccac cctcgtgacc
accttcggct acggcctgca 1920gtgcttcgcc cgctaccccg accacatgaa
gcagcacgac ttcttcaagt ccgccatgcc 1980cgaaggctac gtccaggagc
gcaccatctt cttcaaggac gacggcaact acaagacccg 2040cgccgaggtg
aagttcgagg gcgacaccct ggtgaaccgc atcgagctga agggcatcga
2100cttcaaggag gacggcaaca tcctggggca caagctggag tacaactaca
acagccacaa 2160cgtctatatc atggccgaca agcagaagaa cggcatcaag
gtgaacttca agatccgcca 2220caacatcgag gacggcagcg tgcagctcgc
cgaccactac cagcagaaca cccccatcgg 2280cgacggcccc gtgctgctgc
ccgacaacca ctacctgagc taccagtccg ccctgagcaa 2340agaccccaac
gagaagcgcg atcacatggt cctgctggag ttcgtgaccg ccgccgggat
2400cactctcggc atggacgagc tgtacaagta atcggccgct aatcagccat
accacatttg 2460tagaggtttt acttgcttta aaaaacctcc cacacctccc
cctgaacctg aaacataaaa 2520tgaatgcaat tgttgttgtt aacttgttta
ttgcagctta taatggttac aaataaagca 2580atagcatcac aaatttcaca
aataaagcat ttttttcact gcattctagt tgtggtttgt 2640ccaaactcat
caatgtatct tatcatgtc 2669472992DNAArtificial sequencesynthetic
47gttgacattg attattgact agttattaat agtaatcaat tacggggtca ttagttcata
60gcccatatat ggagttccgc gttacataac ttacggtaaa tggcccgcct ggctgaccgc
120ccaacgaccc ccgcccattg acgtcaataa tgacgtatgt tcccatagta
acgccaatag 180ggactttcca ttgacgtcaa tgggtggagt atttacggta
aactgcccac ttggcagtac 240atcaagtgta tcatatgcca agtacgcccc
ctattgacgt caatgacggt aaatggcccg 300cctggcatta tgcccagtac
atgaccttat gggactttcc tacttggcag tacatctacg 360tattagtcat
cgctattacc atggtgatgc ggttttggca gtacatcaat gggcgtggat
420agcggtttga ctcacgggga tttccaagtc tccaccccat tgacgtcaat
gggagtttgt 480tttggcacca aaatcaacgg gactttccaa aatgtcgtaa
caactccgcc ccattgacgc 540aaatgggcgg taggcgtgta cggtgggagg
tctatataag cagagctctc cctatcagtg 600atagagatct ccctatcagt
gatagagatc gtcgacgttt agtgaaccgt cagatcgcct 660ggagacgcca
tccacgctgt tttgacctcc atagaagaca ccgggaccga tccagcctcc
720gcggccggga acggtgcatt ggaacgcgga ttccccgtgc caagagtgac
gtaagtaccg 780cctatagagt ctataggccc acccccttgg cttcttatgc
atgctatact gtttttggct 840tggggtctat acacccccgc ttcctcatgt
tataggtgat ggtatagctt agcctatagg 900tgtgggttat tgaccattat
tgaccactcc cctattggtg acgatacttt ccattactaa 960tccataacat
ggctctttgc cacaactctc tttattggct atatgccaat acactgtcct
1020tcagagactg acacggactc tgtattttta caggatgggg tctcatttat
tatttacaaa 1080ttcacatata caacaccacc gtccccagtg cccgcagttt
ttattaaaca taacgtggga 1140tctccacgcg aatctcgggt acgtgttccg
gacatggtct cttctccggt agcggcggag 1200cttctacatc cgagccctgc
tcccatgcct ccagcgactc atggtcgctc ggcagctcct 1260tgctcctaac
agtggaggcc agacttaggc acagcacgat gcccaccacc accagtgtgc
1320cgcacaaggc cgtggcggta gggtatgtgt ctgaaaatga gctcggggag
cgggcttgca 1380ccgctgacgc atttggaaga cttaaggcag cggcagaaga
agatgcaggc agctgagttg 1440ttgtgttctg ataagagtca gaggtaactc
ccgttgcggt gctgttaacg gtggagggca 1500gtgtagtctg agcagtactc
gttgctgccg cgcgcgccac cagacataat agctgacaga 1560ctaacagact
gttcctttcc atgggtcttt tctgcagaag cttatactcg agctctagat
1620tgggaacccg ggtctctcga attcgagatc tccaccatgc acagacctag
acgtcgtgga 1680actcgtccac ctccactggc actgctcgct gctctcctcc
tggctgcacg tggtgctgat 1740gcagaggtgc agctggtgga gtctggggga
gccatagtaa agccgggggg gtcccataga 1800gtctcctgtg aagcctctgg
attcactttc agtaacgcct ggatgagttg ggtccgccag 1860gctccaggga
gggggctgga gtgggttggc cgtattttaa gcaagactga tggtgggacg
1920acagactacg ctgcacccgt gaaagacaga ttcaccattt caagagatga
ttctaaaaat 1980atgttgtttc tgcaaatgga cagcctgaaa atcgaggaca
cagccgtgta tttctgtacc 2040acggccgatt tttggagtgc ttattcttct
gactactggg gccagggaac cctggtcacc 2100gtctcctcag gaggtggagg
ttccgggggc gggggctccg gcggaggtgg atcagatatt 2160gtgatgactc
agtctccact ctccctgccc gtcacccctg gagagccggc ctccatctcc
2220tgcaggtcta gtcagagcct cctgcatagt aatgggtaca actatttgga
ttggtaccta 2280cagaagccag ggcagtctcc acaactcctg atctatttgg
gttctaatcg ggcctccggg 2340gtccctgaca ggttcagtgg cagtggatca
ggcacagatt ttacactgaa aatcagcaga 2400atggaggctg aggatgttgg
ggtttattac tgcatgcaag gtctacaaac tccgtacact 2460tttggccagg
ggaccaagct ggagatcaaa ggaggcggag ggagtgtttt gttttatctg
2520gccgttggga taatgtttct cgtaaataca gtactttggg taacaataag
gaaggaactg 2580aagagaaaga aaaaatggga tctggaaata tcattggaca
gtggacacga aaaaaaagtc 2640acatcatcat tgcaagaaga ccggcacttg
gaggaggaac tgaaatgtca agagcaaaaa 2700gaagaacaac tgcaagaagg
cgtacataga aaagaaccac agggagcaac ataggcggcc 2760gctaatcagc
cataccacat ttgtagaggt tttacttgct ttaaaaaacc tcccacacct
2820ccccctgaac ctgaaacata aaatgaatgc aattgttgtt gttaacttgt
ttattgcagc 2880ttataatggt tacaaataaa gcaatagcat cacaaatttc
acaaataaag catttttttc 2940actgcattct agttgtggtt tgtccaaact
catcaatgta tcttatcatg tc 2992485765DNAArtificial sequencesynthetic
48acaacttcgt atagcataca ttatacgaag ttatggtacc aagcctaggc ctccaaaaaa
60gcctcctcac tacttctgga atagctcaga ggcagaggcg gcctcggcct ctgcataaat
120aaaaaaaatt agtcagccat ggggcggaga atgggcggaa ctgggcggag
ttaggggcgg 180gatgggcgga gttaggggcg ggactatggt tgctgactaa
ttgagatgca tgctttgcat 240acttctgcct gctggggagc ctggggactt
tccacacctg gttgctgact aattgagatg 300catgctttgc atacttctgc
ctgctgggga gcctggggac tttccacacc ggatccacca 360tgggttcagc
tattgagcag gatgggttgc atgctggtag tcccgccgca tgggtcgaac
420gactgtttgg atacgattgg gcccaacaga ctataggctg ttccgacgct
gctgtctttc 480gtctttctgc acaaggtcgt ccagttctgt tcgtgaaaac
cgacttgtcc ggagccctca 540atgagttgca agacgaagct gcacgactga
gttggcttgc caccactggt gtcccatgtg 600ccgcagtact tgacgtcgtc
acagaggctg gtcgcgattg gttgctcctt ggagaagtgc 660ccggccaaga
tcttctcagt tcccaccttg cccctgccga aaaagtttca ataatggctg
720acgctatgag aaggctgcac acccttgacc ctgccacatg tccattcgat
caccaagcca 780aacaccgaat tgaacgagct agaacccgca tggaagccgg
cctcgttgat caagacgatt 840tggatgagga acaccagggt ctcgcacccg
ctgaactctt cgctcgcctc aaagcacgaa 900tgccagacgg agatgacttg
gtcgtaaccc acggagatgc ctgccttcct aacataatgg 960tagagaatgg
aagatttagc ggcttcattg attgtggacg acttggagtt gcagatcggt
1020accaagatat cgctctcgct accagagata ttgctgaaga attgggcgga
gaatgggctg 1080atcggtttct cgtactctac ggaattgccg cacctgattc
ccaacgcatt gctttttacc 1140gtcttctgga tgagttcttc taaacgcgtc
ccccctctcc ctcccccccc cctaacgtta 1200ctggccgaag ccgcttggaa
taaggccggt gtgcgtttgt ctatatgtta ttttccacca 1260tattgccgtc
ttttggcaat gtgagggccc ggaaacctgg ccctgtcttc ttgacgagca
1320ttcctagggg tctttcccct ctcgccaaag gaatgcaagg tctgttgaat
gtcgtgaagg 1380aagcagttcc tctggaagct tcttgaagac aaacaacgtc
tgtagcgacc ctttgcaggc 1440agcggaaccc cccacctggc gacaggtgcc
tctgcggcca aaagccacgt gtataagata 1500cacctgcaaa ggcggcacaa
ccccagtgcc acgttgtgag ttggatagtt gtggaaagag 1560tcaaatggct
ctcctcaagc gtattcaaca aggggctgaa ggatgcccag aaggtacccc
1620attgtatggg atctgatctg gggcctcggt gcacatgctt tacatgtgtt
tagtcgaggt 1680taaaaaacgt ctaggccccc cgaaccacgg ggacgtggtt
ttcctttgaa aaacacgatt 1740gctcgaatca ccatggtgag caagggcgag
gagctgttca ccggggtggt gcccatcctg 1800gtcgagctgg acggcgacgt
aaacggccac aagttcagcg tgtccggcga gggcgagggc 1860gatgccacct
acggcaagct gaccctgaag ttcatctgca ccaccggcaa gctgcccgtg
1920ccctggccca ccctcgtgac caccttcggc tacggcctgc agtgcttcgc
ccgctacccc 1980gaccacatga agcagcacga cttcttcaag tccgccatgc
ccgaaggcta cgtccaggag 2040cgcaccatct tcttcaagga cgacggcaac
tacaagaccc gcgccgaggt gaagttcgag 2100ggcgacaccc tggtgaaccg
catcgagctg aagggcatcg acttcaagga ggacggcaac 2160atcctggggc
acaagctgga gtacaactac aacagccaca acgtctatat catggccgac
2220aagcagaaga acggcatcaa ggtgaacttc aagatccgcc acaacatcga
ggacggcagc 2280gtgcagctcg ccgaccacta ccagcagaac acccccatcg
gcgacggccc cgtgctgctg 2340cccgacaacc actacctgag ctaccagtcc
gccctgagca aagaccccaa cgagaagcgc 2400gatcacatgg tcctgctgga
gttcgtgacc gccgccggga tcactctcgg catggacgag 2460ctgtacaagt
aatcggccgc taatcagcca taccacattt gtagaggttt tacttgcttt
2520aaaaaacctc ccacacctcc ccctgaacct gaaacataaa atgaatgcaa
ttgttgttgt 2580taacttgttt attgcagctt ataatggtta caaataaagc
aatagcatca caaatttcac 2640aaataaagca tttttttcac tgcattctag
ttgtggtttg tccaaactca tcaatgtatc 2700ttatcatgtc ggcgcgttga
cattgattat tgactagtta ttaatagtaa tcaattacgg 2760ggtcattagt
tcatagccca tatatggagt tccgcgttac ataacttacg gtaaatggcc
2820cgcctggctg accgcccaac gacccccgcc cattgacgtc aataatgacg
tatgttccca 2880tagtaacgcc aatagggact ttccattgac gtcaatgggt
ggagtattta cggtaaactg 2940cccacttggc agtacatcaa gtgtatcata
tgccaagtac gccccctatt gacgtcaatg 3000acggtaaatg gcccgcctgg
cattatgccc agtacatgac cttatgggac tttcctactt 3060ggcagtacat
ctacgtatta gtcatcgcta ttaccatggt gatgcggttt tggcagtaca
3120tcaatgggcg tggatagcgg tttgactcac ggggatttcc aagtctccac
cccattgacg 3180tcaatgggag tttgttttgg caccaaaatc aacgggactt
tccaaaatgt cgtaacaact 3240ccgccccatt gacgcaaatg ggcggtaggc
gtgtacggtg ggaggtctat ataagcagag 3300ctctccctat cagtgataga
gatctcccta tcagtgatag agatcgtcga cgtttagtga 3360accgtcagat
cgcctggaga cgccatccac gctgttttga cctccataga agacaccggg
3420accgatccag cctccgcggc cgggaacggt gcattggaac gcggattccc
cgtgccaaga 3480gtgacgtaag taccgcctat agagtctata ggcccacccc
cttggcttct tatgcatgct 3540atactgtttt tggcttgggg tctatacacc
cccgcttcct catgttatag gtgatggtat 3600agcttagcct ataggtgtgg
gttattgacc attattgacc actcccctat tggtgacgat 3660actttccatt
actaatccat aacatggctc tttgccacaa ctctctttat tggctatatg
3720ccaatacact gtccttcaga gactgacacg gactctgtat ttttacagga
tggggtctca 3780tttattattt acaaattcac atatacaaca ccaccgtccc
cagtgcccgc agtttttatt 3840aaacataacg tgggatctcc acgcgaatct
cgggtacgtg ttccggacat ggtctcttct 3900ccggtagcgg cggagcttct
acatccgagc cctgctccca tgcctccagc gactcatggt 3960cgctcggcag
ctccttgctc ctaacagtgg aggccagact taggcacagc acgatgccca
4020ccaccaccag tgtgccgcac aaggccgtgg cggtagggta tgtgtctgaa
aatgagctcg 4080gggagcgggc ttgcaccgct gacgcatttg gaagacttaa
ggcagcggca gaagaagatg 4140caggcagctg agttgttgtg ttctgataag
agtcagaggt aactcccgtt gcggtgctgt 4200taacggtgga gggcagtgta
gtctgagcag tactcgttgc tgccgcgcgc gccaccagac 4260ataatagctg
acagactaac agactgttcc tttccatggg tcttttctgc agtcaccgtc
4320cttgacacga agcttatact cgagctctag attgggaacc cgggtctctc
gaattcgaga 4380tctccaccat gcacagacct agacgtcgtg gaactcgtcc
acctccactg gcactgctcg 4440ctgctctcct cctggctgca cgtggtgctg
atgcagaggt gcagctggtg gagtctgggg 4500gagccatagt aaagccgggg
gggtcccata gagtctcctg tgaagcctct ggattcactt 4560tcagtaacgc
ctggatgagt tgggtccgcc aggctccagg gagggggctg gagtgggttg
4620gccgtatttt aagcaagact gatggtggga cgacagacta cgctgcaccc
gtgaaagaca 4680gattcaccat ttcaagagat gattctaaaa atatgttgtt
tctgcaaatg gacagcctga 4740aaatcgagga cacagccgtg tatttctgta
ccacggccga tttttggagt gcttattctt 4800ctgactactg gggccaggga
accctggtca ccgtctcctc aggaggtgga ggttccgggg 4860gcgggggctc
cggcggaggt ggatcagata ttgtgatgac tcagtctcca ctctccctgc
4920ccgtcacccc tggagagccg gcctccatct cctgcaggtc tagtcagagc
ctcctgcata 4980gtaatgggta caactatttg gattggtacc tacagaagcc
agggcagtct ccacaactcc 5040tgatctattt gggttctaat cgggcctccg
gggtccctga caggttcagt ggcagtggat 5100caggcacaga ttttacactg
aaaatcagca gaatggaggc tgaggatgtt ggggtttatt 5160actgcatgca
aggtctacaa actccgtaca cttttggcca ggggaccaag ctggagatca
5220aaggaggcgg agggagtgtt ttgttttatc tggccgttgg gataatgttt
ctcgtaaata 5280cagtactttg ggtaacaata aggaaggaac tgaagagaaa
gaaaaaatgg gatctggaaa 5340tatcattgga cagtggacac gaaaaaaaag
tcacatcatc attgcaagaa gaccggcact 5400tggaggagga actgaaatgt
caagagcaaa aagaagaaca actgcaagaa ggcgtacata 5460gaaaagaacc
acagggagca acataggcgg ccgctaatca gccataccac atttgtagag
5520gttttacttg ctttaaaaaa cctcccacac ctccccctga acctgaaaca
taaaatgaat 5580gcaattgttg ttgttaactt gtttattgca gcttataatg
gttacaaata aagcaatagc 5640atcacaaatt tcacaaataa agcatttttt
tcactgcatt ctagttgtgg tttgtccaaa 5700ctcatcaatg tatcttatca
tgtctaccgg tataacttcg tataatgtat actatacgaa 5760gttag
576549660DNAArtificial sequencesynthetic 49gacatcgtga tgacccagtc
tccactctcc ctgcccgtca cccctggaga gccggcctcc 60atctcctgca ggtctagtca
gagcctcctg catagtaatg ggtacaacta tttggattgg 120tacctacaga
agccagggca gtctccacaa ctcctgatct atttgggttc taatcgggcc
180tccggggtcc ctgacaggtt cagtggcagt ggatcaggca cagattttac
actgaaaatc 240agcagaatgg aggctgagga tgttggggtt tattactgca
tgcaaggtct acaaactccg 300tacacttttg gccaggggac caagctggag
atcaaacgag ctgatgctgc accaactgta 360tccatcttcc caccatccag
tgagcagtta acatctggag gtgcctcagt cgtgtgcttc 420ttgaacaact
tctaccccaa agacatcaat gtcaagtgga agattgatgg cagtgaacga
480caaaatggcg tcctgaacag ttggactgat caggacagca aagacagcac
ctacagcatg 540agcagcaccc tcacgttgac caaggacgag tatgaacgac
ataacagcta tacctgtgag 600gccactcaca agacatcaac ttcacccatt
gtcaagagct tcaacagggg agagtgttga 660501359DNAArtificial
sequencesynthetic 50gaggtgcagc tggtggagtc tgggggagcc atagtaaagc
cgggggggtc ccatagagtc 60tcctgtgaag cctctggatt cactttcagt aacgcctgga
tgagttgggt ccgccaggct 120ccagggaggg ggctggagtg ggttggccgt
attttaagca agactgatgg tgggacgaca 180gactacgctg cacccgtgaa
agacagattc accatttcaa gagatgattc taaaaatatg 240ttgtttctgc
aaatggacag cctgaaaatc gaggacacag ccgtgtattt ctgtaccacg
300gccgattttt ggagtgctta ttcttctgac tactggggcc agggaaccct
ggtcaccgtc 360tcctcagcca aaacaacagc cccatcggtc tatccactgg
cccctgtgtg tggagataca 420actggctcct cggtgactct aggatgcctg
gtcaagggtt atttccctga gccagtgacc 480ttgacctgga actctggatc
cctgtccagt ggtgtgcaca ccttcccagc tgtcctgcag 540tctgacctct
acaccctcag cagctcagtg actgtaacct cgagcacctg gcccagccag
600tccatcacct gcaatgtggc ccacccggca agcagcacca aggtggacaa
gaaaattgag 660cccagagggc ccacaatcaa gccctgtcct ccatgcaaat
gcccagcacc taacctcttg 720ggtggaccat ccgtcttcat cttccctcca
aagatcaagg atgtactcat gatctccctg 780agccccatag tcacatgtgt
ggtggtggat gtgagcgagg atgacccaga tgtccagatc 840agctggtttg
tgaacaacgt ggaagtacac acagctcaga cacaaaccca tagagaggat
900tacaacagta ctctccgggt ggtcagtgcc ctccccatcc agcaccagga
ctggatgagt 960ggcaaggagt tcaaatgcaa ggtcaacaac aaagacctcc
cagcgcccat cgagagaacc 1020atctcaaaac ccaaagggtc agtaagagct
ccacaggtat atgtcttgcc tccaccagaa 1080gaagagatga ctaagaaaca
ggtcactctg acctgcatgg tcacagactt catgcctgaa 1140gacatttacg
tggagtggac caacaacggg aaaacagagc taaactacaa gaacactgaa
1200ccagtcctgg actctgatgg ttcttacttc atgtacagca agctgagagt
ggaaaagaag 1260aactgggtgg aaagaaatag ctactcctgt tcagtggtcc
acgagggtct gcacaatcac 1320cacacgacta agagcttctc ccggactccg
ggtaaatga 1359511011DNAArtificial sequencesynthetic 51gaggtgcagc
tggtggagtc tgggggagcc atagtaaagc cgggggggtc ccatagagtc 60tcctgtgaag
cctctggatt cactttcagt aacgcctgga tgagttgggt ccgccaggct
120ccagggaggg ggctggagtg ggttggccgt attttaagca agactgatgg
tgggacgaca 180gactacgctg cacccgtgaa agacagattc accatttcaa
gagatgattc taaaaatatg 240ttgtttctgc aaatggacag cctgaaaatc
gaggacacag ccgtgtattt ctgtaccacg 300gccgattttt ggagtgctta
ttcttctgac tactggggcc agggaaccct ggtcaccgtc 360tcctcaggag
gtggaggttc cgggggcggg ggctccggcg gaggtggatc agatattgtg
420atgactcagt ctccactctc cctgcccgtc acccctggag agccggcctc
catctcctgc 480aggtctagtc agagcctcct gcatagtaat gggtacaact
atttggattg gtacctacag 540aagccagggc agtctccaca actcctgatc
tatttgggtt ctaatcgggc ctccggggtc 600cctgacaggt tcagtggcag
tggatcaggc acagatttta cactgaaaat cagcagaatg 660gaggctgagg
atgttggggt ttattactgc atgcaaggtc tacaaactcc gtacactttt
720ggccagggga ccaagctgga gatcaaagga ggcggaggga gtgttttgtt
ttatctggcc 780gttgggataa tgtttctcgt aaatacagta ctttgggtaa
caataaggaa ggaactgaag 840agaaagaaaa aatgggatct ggaaatatca
ttggacagtg gacacgaaaa aaaagtcaca 900tcatcattgc aagaagaccg
gcacttggag gaggaactga aatgtcaaga gcaaaaagaa 960gaacaactgc
aagaaggcgt acatagaaaa gaaccacagg gagcaacata g 1011
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